Public Policy in ALS/MND Care: An International Perspective [1st ed.] 9789811558399, 9789811558405

Table of contents :
Front Matter ....Pages i-xxxi
Introduction to Public Policy of ALS/MND (Jerome E. Kurent, David Oliver, Robert H. Blank)....Pages 1-28
Public Policy in MND Care: The Australian Perspective (Samar Aoun, Carol Birks, Anne Hogden, Susan Mathers)....Pages 29-49
Public Policy in ALD/MND Care: The Belgian Perspective (Evy Reviers, Ludo Vanopdenbosch, Ludo Van Den Bosch, Philip Van Damme)....Pages 51-63
Amyotrophic Lateral Sclerosis in Brazil (Tauana Bernardes Leoni, Marcondes C. França Jr.)....Pages 65-76
Public Policy of ALS in Canada (Wendy S. Johnston, Westerly Luth)....Pages 77-96
Public Policy for Amyotrophic Lateral Sclerosis in China (Lu Chen, Dongsheng Fan)....Pages 97-106
German Perspective on ALS/MND Policy (Maike F. Dohrn, Roman Rolke)....Pages 107-120
Living and Dying with ALS/MND in India: Public Policy and Private Realities (Roop Gursahani, Satish Khadilkar)....Pages 121-129
The Experience of Amyotrophic Lateral Sclerosis in Ireland (Orla Hardiman, Stela Lefter, Miriam Galvin)....Pages 131-148
Public Policy of ALS Care in Israel (Marc Gotkine, Efrat Carmi)....Pages 149-162
Public Policy in ALS Care: The Italian Situation (Simone Veronese, Andrea Calvo)....Pages 163-175
ALS Policy: A Japanese Perspective (Mieko Ogino, Tamerlan Babayev)....Pages 177-189
ALS Policy in Mexico (Ildefonso Rodriguez-Leyva)....Pages 191-199
Public Policy in MND Care: Nigerian Perspective (Yomi Ogun, Babawale Arabambi)....Pages 201-208
Public Policy of ALS: A Pakistani Perspective (Asfandyar Khan Niazi, Aqdas Kazi, Arsalan Ahmad)....Pages 209-217
Public Policy in ALS Care: The Polish Perspective (Anna Adamczyk, Wojciech Leppert)....Pages 219-226
ALS Policy: A Russian Perspective (L. V. Brylev, D. V. Nevzorova, M. N. Zakharova, A. B. Guekht)....Pages 227-231
Public Policy in ALS/MND Care: South African Perspective (Jeannine M. Heckmann, Alexandra S. Amaler)....Pages 233-246
Public Policy in ALS Care: South Korea (Seung Hyun Kim, Kiwook Oh, Bugyeong Son)....Pages 247-261
Amyotrophic Lateral Sclerosis Care in Tunisia (Imen Kacem, Ikram Sghaier, Amina Nasri, Riadh Gouider)....Pages 263-278
Public Policy in MND Care: The United Kingdom (David Oliver, Christopher McDermott)....Pages 279-300
ALS Public Policy in the United States (Benjamin Rix Brooks, Jerome E. Kurent)....Pages 301-326
Conclusions: What We Can Learn from the Country Perspectives (Robert H. Blank, Jerome E. Kurent, David Oliver)....Pages 327-345

Citation preview

Public Policy in ALS/MND Care An International Perspective Edited by  Robert H. Blank · Jerome E. Kurent · David Oliver

Public Policy in ALS/MND Care

Robert H. Blank Jerome E. Kurent  •  David Oliver Editors

Public Policy in ALS/MND Care An International Perspective

Editors Robert H. Blank University of Canterbury, Christchurch, New Zealand

Jerome E. Kurent Medical University of South Carolina Charleston, SC, USA

David Oliver University of Kent Canterbury, UK

ISBN 978-981-15-5839-9    ISBN 978-981-15-5840-5 (eBook) https://doi.org/10.1007/978-981-15-5840-5 © The Editor(s) (if applicable) and The Author(s), under exclusive licence to Springer Nature Singapore Pte Ltd. 2021 This work is subject to copyright. All rights are solely and exclusively licensed by the Publisher, whether the whole or part of the material is concerned, specifically the rights of translation, reprinting, reuse of illustrations, recitation, broadcasting, reproduction on microfilms or in any other physical way, and transmission or information storage and retrieval, electronic adaptation, computer software, or by similar or dissimilar methodology now known or hereafter developed. The use of general descriptive names, registered names, trademarks, service marks, etc. in this publication does not imply, even in the absence of a specific statement, that such names are exempt from the relevant protective laws and regulations and therefore free for general use. The publisher, the authors and the editors are safe to assume that the advice and information in this book are believed to be true and accurate at the date of publication. Neither the publisher nor the authors or the editors give a warranty, expressed or implied, with respect to the material contained herein or for any errors or omissions that may have been made. The publisher remains neutral with regard to jurisdictional claims in published maps and institutional affiliations. Cover illustration: © Ed Reschke/Getty Images This Palgrave Macmillan imprint is published by the registered company Springer Nature Singapore Pte Ltd. The registered company address is: 152 Beach Road, #21-­01/04 Gateway East, Singapore 189721, Singapore

Foreword

When I was a neuromuscular fellow back in 1980, I would observe how my mentors, Drs. Walter G. Bradley and Theodore L. Munsat, managed their ALS Clinic and early clinical trials. Because I was concentrating on basic research, I did not know the factors involved in running clinical programs. I have to admit I did not pay much attention to administration, as these issues were neither clinical nor scientific. A few years later when I wanted to start a multidisciplinary ALS Clinic, I struggled to learn how to do it successfully. This knowledge was clearly over my head. When I wanted to conduct my first clinical trial with thyrotropin-­ releasing hormone (TRH), I would not have been able to accomplish this task without the support and assistance of my chairman Dr. John P. Conomy and his capable administrative assistant. I learned and started this process from scratch. In those days, public policies and the overall infrastructure for ALS was still in the early stages of development. I have to say that since then we have come a long way! We have many multidisciplinary ALS Clinics throughout many parts of the world. However, there are still some areas that lack these clinics. I often use the word, “ALS Community,” which I believe includes people with ALS (PALS) and their family caregivers; doctors, clinicians, any scientists who are involved in the field; hospice and home care agencies; voluntary disease organizations and advocacy groups; investigator-initiated study groups; clinical trial consortia; the National ALS Registry; ALS-specific annual symposium organizers; funding agencies for research and patient care; federal health agencies; policy makers; regulatory agencies; pharmaceutical companies; and new v

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biotech companies. All these stakeholders are working to improve ALS care and research to help combat this “intractable” disease. In 2003, I was asked to assemble a new committee to promote excellence in end-of-life care among PALS by the Robert Wood Johnson Foundation and ALS Association. We published the committee’s recommendations in 2005 and pointed to the need for improvement in public policies, more overall research in ALS, and the dissemination of key information (1). In 2011, I organized an international conference to promote clinical and patient-oriented research to identify the pathogenesis of ALS with the support of many funding agencies and pharmaceutical companies (ALS Community). Prof. Martin Turner and I published a conference supplement in 2013  in the journal Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. There were two articles that were devoted to discussing infrastructure and resources. Dr. Alexander V. Sherman and his colleagues reviewed public policies for funding agencies and discussed overall infrastructure resources for clinical research in ALS (2). Key infrastructure included ALS Clinics, brain banks, the National ALS Registry, and study consortia in the United States and Europe. Dr. David A. Chad also reviewed “Funding agencies and disease organizations: resources and recommendations to facilitate ALS clinical research” (3). Our efforts are still largely fragmented, and at times, I wonder if we may need to repeat our messages over and over again. It has now been ten years since the international conference. I must admit that management and care for PALS is much more complicated due to a multitude of health insurance companies, health care agencies, and palliative care and hospice providers. Movements such as “right to try” and “right to die” also require a great deal of knowledge. The number of ALS clinics has really grown in the United States, Canada, Europe, and Pan-Asian countries. These clinics have become more comprehensive, as they provide the best care for patients and conduct extensive clinical research including clinical trials. Our ultimate goal is to find the cause and pathogenesis of ALS to develop a cure. In the meantime, we must develop medications to markedly slow down the disease. We also need to develop interventions to improve difficult symptoms in ALS, so PALS can maintain their quality of life for as long as possible. Again, the ALS Community as a whole is working toward these objectives. As I experienced many years ago, young energetic doctors and researchers are immediately confronted with a lack of knowledge on public policies and overall complex infrastructure even within the small world of ALS.  I must admit knowledge of public policies in ALS health care has

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grown into a far more complicated web with an overwhelming amount of information. Some countries are more efficient and have great infrastructure, whereas other countries may not be as developed. Furthermore, effective implementation of this information is not easy. Some health agency workers or officials, government or non-­ government, may attempt to improve their policies and infrastructure for the benefits of PALS. Yet, if there are no data available, any improvement will be challenging. There are many ALS books on science and clinical care which have been published in the past, but there is a paucity of information on public policies and beyond, as well as the infrastructure for ALS care and research. When I heard the plan for this book and its focus on public policies and infrastructure for the ALS Community (versus science or patient care), I was so excited, because I feel it is truly needed. The editors of this book include Dr. Robert Blank, a world expert on public policies and health care delivery systems; Dr. Jerome Kurent, a doctor who is most respected for compassion and humanistic care for PALS and their caregivers; and Dr. David Oliver, a doctor who introduced the concept of palliative care for PALS and successfully implemented it. The authors are among the world experts of ALS across 21 countries and provide commentary on their own countries’ health policies and infrastructure for ALS. The title of the book is Public Policies in ALS/MND Care. Yet, I believe this book also covers broader issues that we need to know that go beyond research when treating PALS from diagnosis to end-of-life care. One of the most important goals of this book is to provide the most comprehensive view possible of ALS/MND care and policy through commentary on different systems across 21 countries and beyond. When we face the impossible feat of finding the solution for ALS, we need to take a moment and critically evaluate the field. This book will give us the opportunity to really understand where the field stands and how we can move forward. The impact of this book will be wide-ranging, as it provides the most thorough and broad view of ALS/MND care and policy—not just locally but around the world. This is indeed the first book of its kind. I would like to provide my heartfelt congratulations to the editors and authors, who provided this crucial information and have addressed gaps in knowledge within the field. This is an essential book to read for any stakeholder in ALS. Wesley J Howe Professor of Neurology (at CUIMC) Columbia University Irving Medical Center New York, NY March, 2020

Hiroshi Mitsumoto

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References Mitsumoto, H., M. Bromberg, W. Johnston, R. Tandan et al. (2005). Promoting excellence in end-of-life care in ALS. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 6 (3): 145–54. Sherman, A.V., A.K. Gubitz, A. Al-Chalabi, R. Bedlack et al. (2013). Infrastructure resources for clinical research in amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 14 (Suppl 1): 53–61. Chad, D.A., S. Bidichandani, L. Bruijn, J.D. Capra et al. (2013). Funding agencies and disease organizations: Resources and recommendations to facilitate ALS clinical research. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 14 (Suppl 1): 62–66.

Preface

This book was first proposed by the three editors to be a co-authored volume on ALS/MND public policy in the United Kingdom and the United States. Thanks to an astute reviewer who suggested involving additional countries, we decided to develop an edited multi-authored volume which includes a broad range of contributors from across the globe. We were soon encouraged by the enthusiasm of the many ALS/MND experts willing to participate in this project, including representation from countries often overlooked in comparative studies. Authors from twenty-one countries were requested to describe the current state of ALS/MND public policy as well as implications for patient care. This book focuses on the public policy and ethical dimensions of ALS/ MND care. Policy issues include adequacy of funding for patient care and research, payment policy and regulatory functions of public and private insurers, long-term services and caregiver support, access to genetic testing and assistive technologies, and ensuring a competent and adequate workforce, especially for hands-on caregivers. There also are numerous challenges related to providing palliative and hospice care for patients with ALS/MND, as well as use of advance directives and the highly controversial area of assisted suicide. These are matters that confront policy makers in almost all geographic regions and were addressed whenever possible by each author. To provide a starting point for coverage and to facilitate evaluation of comparative data, chapter contributors were asked to address a series of questions and issues (these are enumerated in Chapter 1) that embody a wide range of policy issues. To avoid repetition while maintaining the ix

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primary focus on policy, authors were requested not to include general background coverage of ALS/MND since this is provided in the introductory chapter along with policy themes of the book. A concluding chapter written by the editors examines the collective findings from the disparate countries represented in this book. Hopefully, this discussion will serve to facilitate workable and humane ALS/MND public policy for patient care and caregiver support in the coming decades. Overall, we argue for approaches that are both multidisciplinary and international. We are indebted to the more than fifty authors who provided their expertise and insights of ALS/MND in producing the chapters that made this book a reality. We especially thank Professor Hiroshi Mitsumoto of Columbia Presbyterian Hospital for his invaluable assistance on this project and for writing the Foreword. We also thank Mr. Anushangi Weerakoon at Palgrave Macmillan Publishing for his enthusiastic support of the book’s concept and for his encouragement over the duration of this project. We dedicate this book to patients with ALS/MND and their families across the globe, and to provide hope for the future of eventually conquering this group of tragic disorders. Sarasota, FL Charleston, SC  Canterbury, UK 

Robert H. Blank Jerome E. Kurent David Oliver

Contents

1 Introduction to Public Policy of ALS/MND  1 Jerome E. Kurent, David Oliver, and Robert H. Blank 2 Public Policy in MND Care: The Australian Perspective 29 Samar Aoun, Carol Birks, Anne Hogden, and Susan Mathers 3 Public Policy in ALD/MND Care: The Belgian Perspective 51 Evy Reviers, Ludo Vanopdenbosch, Ludo Van Den Bosch, and Philip Van Damme 4 Amyotrophic Lateral Sclerosis in Brazil 65 Tauana Bernardes Leoni and Marcondes C. França Jr. 5 Public Policy of ALS in Canada 77 Wendy S. Johnston and Westerly Luth 6 Public Policy for Amyotrophic Lateral Sclerosis in China 97 Lu Chen and Dongsheng Fan

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7 German Perspective on ALS/MND Policy107 Maike F. Dohrn and Roman Rolke 8 Living and Dying with ALS/MND in India: Public Policy and Private Realities121 Roop Gursahani and Satish Khadilkar 9 The Experience of Amyotrophic Lateral Sclerosis in Ireland131 Orla Hardiman, Stela Lefter, and Miriam Galvin 10 Public Policy of ALS Care in Israel149 Marc Gotkine and Efrat Carmi 11 Public Policy in ALS Care: The Italian Situation163 Simone Veronese and Andrea Calvo 12 ALS Policy: A Japanese Perspective177 Mieko Ogino and Tamerlan Babayev 13 ALS Policy in Mexico191 Ildefonso Rodriguez-Leyva 14 Public Policy in MND Care: Nigerian Perspective201 Yomi Ogun and Babawale Arabambi 15 Public Policy of ALS: A Pakistani Perspective209 Asfandyar Khan Niazi, Aqdas Kazi, and Arsalan Ahmad 16 Public Policy in ALS Care: The Polish Perspective219 Anna Adamczyk and Wojciech Leppert

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17 ALS Policy: A Russian Perspective227 L. V. Brylev, D. V. Nevzorova, M. N. Zakharova, and A. B. Guekht 18 Public Policy in ALS/MND Care: South African Perspective233 Jeannine M. Heckmann and Alexandra S. Amaler 19 Public Policy in ALS Care: South Korea247 Seung Hyun Kim, Kiwook Oh, and Bugyeong Son 20 Amyotrophic Lateral Sclerosis Care in Tunisia263 Imen Kacem, Ikram Sghaier, Amina Nasri, and Riadh Gouider 21 Public Policy in MND Care: The United Kingdom279 David Oliver and Christopher McDermott 22 ALS Public Policy in the United States301 Benjamin Rix Brooks and Jerome E. Kurent 23 Conclusions: What We Can Learn from the Country Perspectives327 Robert H. Blank, Jerome E. Kurent, and David Oliver

Notes on Contributors

Anna Adamczyk  is a specialist in neurology and in palliative medicine. She is Head of the Department of Palliative Medicine at the University Hospital No. 1  in Clinical Hospital in Bydgoszcz and a lecturer at the Department of Palliative Care at the Ludwik Rydygier Collegium Medicum in Bydgoszcz of the Nicolaus Copernicus University in Toruń. She works within palliative medicine, and practices as a neurologist, with an interest in caring for patients with diseases of the nervous system, particularly amyotrophic lateral sclerosis, and in the treatment of neuropathic pain. Arsalan Ahmad  MBBS, MD (Neurology), is Professor of Neurology at Shifa International Hospital, Shifa Tameer-e-Millat University, Islamabad, Pakistan. He completed his MBBS from Dow Medical College in 1990 and Doctor of Medicine in Neurology in 2000. He joined Shifa International Hospital in 2003 and was Head of Neurology from 2005 to 2009 and 2012. He was President of Pakistan Society of Neurology from 2016–2018 and President of Movement Disorders Society Pakistan from 2018–2020. He has an interest in movement disorders, neuromuscular disorders and neurogenetics. He has over 100 publications and abstracts including two articles on familial ALS in The Neurogenetics Journal. Alexandra  S.  Amaler  is a final year postgraduate law student at the University of Cape Town, who completed her moot on the question of assisted dying with respect to ALS.

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Samar Aoun  is Professor of Palliative Care Research. She adopts a public health approach and a focus on under-served population groups such as people with MND and advocates for person-centred health and social care. Her research programs on supporting family caregivers at end of life and the Public Health Model of Bereavement Support have informed policy and practice at the national and international levels. She chairs the MND Association in Western Australia, is a director on the board of MND Australia and a member of the scientific committee of MND Research Institute Australia. Babawale  Arabambi  is a neurologist and physician at the Lagos State University Teaching Hospital, Nigeria, with a keen interest in stroke neurology, movement disorders, and clinical neurophysiology. He also co-­ manages the hospital’s neurophysiology laboratory, where he performs and interprets the relevant procedures. He is a recipient of the International Scholarship Award of the American Academy of Neurology for his work on non-motor symptoms of Parkinson’s disease in Nigerian outpatients in 2019. He has also authored/co-authored several publications touching on various fields in neurology. Tamerlan  Babayev  graduated from Imperial College London in 2011 before undertaking postgraduate clinical training in the UK. He moved to Japan in April 2017 to take up an assistant professorship in International University of Health and Welfare and pursue a passion for medical education and research. His contribution to this book stems from an interest in medical ethics and the interplay between culture and healthcare policy. Carol Birks  has worked with people living with MND for over 20 years. She worked initially as manager of support services at MND NSW before becoming CEO of MND Australia in 2006. Her work with MND Australia encompasses influencing government policy to address the complex care needs of people with MND.  Birks was a board member of the International Alliance of ALS/MND Associations from 2010 to 2017, serving as Treasurer and President. Birks has supported new and emerging ALS/MND associations globally, particularly in the Asia Pacific region. Birks is a registered nurse with a graduate diploma in palliative care. Robert H. Blank  PhD, has been Professor of Public Policy at universities in New Zealand (Canterbury), Britain (Brunel) and the U.S. (Idaho and

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Northern Illinois) and a frequent guest professor at Aarhus University in Denmark and National Taiwan University in Taiwan. Among the over forty books he published on comparative health policy, genetic and reproductive policy, and neuroscience policy are Rationing Medicine (Columbia University Press), Brain Policy (Georgetown University Press), Intervention in the Brain (MIT Press), Comparative Health Policy, 1st–5th eds. (Palgrave) and End of Life Decision Making: A Comparative Study (MIT Press). Benjamin  Rix  Brooks MD, is Medical Director of the Carolinas Neuromuscular/ALS–MDA-Care-Center and the Atrium Health ALS Association Certified-Treatment-Center-of-Excellence (CTCE) at the Atrium Health Neurosciences Institute that received the first ever Joint Commission awarded Disease-Specific Care Certification in ALS, and Professor, Department of Neurology, University of North Carolina School of Medicine, Charlotte Campus. Brooks is a founding member of the World Federation of Neurology Research Group on Motor Neuron Diseases leading efforts to design the El Escorial criteria for diagnosis of ALS and the ALS-Functional-Rating-Scale-Revised (ALSFRS-R). In 2012, he received the Forbes Norris Award from The International Alliance of ALS/MND Associations. L. V. Brylev  graduated from the Medical Faculty of Lomonosov Moscow State University in 2004 and completed residency in the Research Center of Neurology RAMS in 2006. He is head of the Department of Neurology at the Buyanov City Hospital, and the Medical Director of “Live now”, a charity foundation for people with ALS.  He is team leader of ALS Center Moscow, part of the European Network to Cure ALS Network, and co-author of Russian Clinical Guidelines on ALS. Andrea Calvo  is Associate Professor of Neurology at the Department of Neurosciences ‘Rita Levi Montalcini’ of the University of Turin. He has been vice-director at Turin ALS Expert Centre since 1997. He is the Co-Chair of the EAN Scientific Panel for ALS and FTD from 2019 and Chair of the Italian Motoneuron Diseases Study Group of the Italian Society of Neurology (SIN). His research interests are in the neurological field, particularly related to ALS and other neuromuscular diseases—epidemiology, clinical genetics, neuroimaging, palliative care, and clinical trials—with 170 papers in international journals.

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Efrat  Carmi is the CEO of IsrALS—The Israeli ALS Research Association--and has been with IsrALS since 2007. IsrALS is the primary organization supporting ALS research and patient care in the country. Efrat got her Psychology degree from Tel Aviv University and her MBA from the University of Central Florida. Efrat is an active member in the ALS/MND International Alliance and has served as a board member of the Alliance for six years. Lu Chen  MD, is a physician in the Department of Neurology, Peking University Third Hospital. Chen got her medical degree from Peking University Health Science Center in 2014. She is focusing on the study of ALS and has published thirty-six peer-reviewed articles. Her representative articles include studies about the natural history and clinical features of patients with ALS in China (JNNP 2015), the prevalence and incidence of ALS in China (JNNP 2020), and the difference in clinical features between German and Chinese ALS patients (J Neurol 2019). Maike F. Dohrn  is a specialist for neuromuscular disorders with a scientific focus on neurogenetics. She collaborated in the neuromuscular outpatient clinic of the RWTH Aachen University hospital as a student before she undertook her resident clinical training in 2015. She has conducted several studies on Charcot-Marie-Tooth disease, hereditary transthyretin amyloidosis, and small fiber neuropathies. Dohrn worked as an intern at the Center for Genomics and Transcriptomics (CeGaT) in Tübingen, Germany, and at the University of Porto, Portugal. Currently, she has a research fellowship at the John P. Hussman Institute for Human Genomics at the University of Miami, Florida. Dongsheng  Fan MD, Professor and Director of the Neurological Department at PUTH, has focused on the study with the aim of curing ALS.  Fan and his colleagues have made great efforts for Chinese ALS patients, including the establishment of the biggest follow-up database in China. Their current works include clinical trial studies, palliative and hospice care, and genetic investigations to find new genes that cause ALS in families. The Neurological Department of PUTH has therefore become a nationally recognized center for research and clinical care in ALS in China.

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Marcondes  C.  França Jr. MD, PhD, is Associate Professor in the Department of Neurology at the School of Medical Sciences at the University of Campinas (UNICAMP), Campinas, Brazil. He is the director of the ALS outpatient clinic at UNICAMP hospital. His research group has been working in the search for neuroimaging biomarkers and in the characterization of the genetic epidemiology of ALS in Brazil. França is the former chair of the Neuromuscular section at the Brazilian Academy of Neurology. He serves on the board of the Brazilian Association of Amyotrophic Lateral Sclerosis (ABrELA). Miriam  Galvin is Associate Professor in Intersectional Research Methodology at the Academic Unit of Neurology, School of Medicine, TCD and Atlantic Senior Fellow for Equity in Brain Health, Global Brain Health Institute. She works across a range of health research projects, mixed methods and qualitative research tracking patient and caregiver journeys, interaction with the health services and the conceptualisation and assessment of quality of life and caregiving experiences. She has a multi-disciplinary academic background in human geography, population health and psychosocial studies, with interests in research methodologies, medical anthropology, and discourse. Marc Gotkine  received his medical degree from King’s College, London. After moving to Israel, he completed his residency in Hadassah University Hospital, Jerusalem. He set up the Hadassah ALS clinic and he also heads the neuromuscular service and EMG lab. The Hadassah ALS clinic serves as an ALS research hub for the whole country both in basic science and clinical trials. He has a special interest in studying the genetics of ALS in Israel, with a focus on ALS in consanguineous families. His other research interests are the genetics and epidemiology of ALS, ALS biomarkers and the microbiome in ALS. Riadh  Gouider is the head of Department of Neurology at Razi University Hospital, the Clinical Investigation Centre (CIC), the Alzheimer’s center and the Multiple Sclerosis Center. He is Trustee of the World Federation of Neurology and Member in the ALS research project and related syndromes in tropical zone (TROPALS). He is a fellow of the European Academy of Neurology as well as the American Academy of Neurology since 2019. He authored and co-authored many original papers or book chapters such as Epidemiology of ALS and Clinical Features of ALS in Africa.

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A. B. Guekht  is the director of the Moscow Research and Clinical Center for Neuropsychiatry and Professor of Neurology at the Russian National Research Medical University. She is the author of more than 200 publications, including more than 90 papers in international peer-­reviewed journals and chapters in international textbooks. She is the Elected Trustee of the World Federation of Neurology, Secretary-General of the National Society of Neurologists and involved in collaborative projects with the World Health Organisation. Roop  Gursahani is a practicing clinical neurologist at P.D. Hinduja National Hospital in Mumbai. He finished formal training and certification in Internal Medicine and then in Neurology by 1988. His special interests include epilepsy and palliative neurology. His advocacy efforts concern end-of-life care in India and include working for appropriate legislation, professional training, and public awareness. He is a member of the steering committee of ELICIT, the interdisciplinary task force of intensivists, palliative care physicians and neurologists for End of Life Care in India. Orla Hardiman  is Professor of Neurology at Trinity College Dublin and Consultant Neurologist at Beaumont Hospital, where she is Director of the National Amyotrophic Lateral Sclerosis service. She is also the National Clinical Lead in Neurology. She is one of only five active clinicians elected to the Royal Irish Academy. She is Editor-in-Chief of the journal Amyotrophic Lateral Sclerosis and the Frontotemporal Degenerations. Her research interests are in clinical phenotyping, epidemiology, genomics, biomarker development and new therapeutics in ALS and related disorders. Jeannine M. Heckmann  MBChB, PhD, is a neurologist in the Division of Neurology at Groote Schuur Hospital and the University of Cape Town, South Africa. Her clinical expertise is in neuromuscular diseases. She established and heads the multi-disciplinary ALS clinic at Groote Schuur Hospital, as well as an ALS research group, which collaborates with international partners. Anne  Hogden  is a Senior Lecturer and researcher with the Australian Institute of Health Service Management. Her research interests are in healthcare communication, patient-centred care and decision-making and interprofessional team processes, with an emphasis on people with life-­ limiting conditions. Anne’s research includes developing web-based decision tools to support people living with ALS/MND to make difficult

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decisions for care and quality of life. Her teaching work is in convening and delivering healthcare safety and quality and research units for the Master of Health Service Management, and supervision of PhD students. Wendy S. Johnston  is Professor Medicine in the Division of Neurology at the Faculty of Medicine and Dentistry at the University of Alberta, Edmonton, Canada. As Medical Director of the University of Alberta Amyotrophic Lateral Sclerosis Programme she leads a multidisciplinary team dedicated to the care of patients with ALS and other motor neuron diseases. Her research encompasses both qualitative research in ALS as well as an active investigational drug trial programme. She serves on the Board of ALS Canada and is past-Chair of the Canadian ALS Clinical Research network. Imen  Kacem is the director of the ALS center in Department of Neurology at Razi University Hospital. She is member in the ALS research project and related syndromes in tropical zone (TROPALS). She won the International Scholarship Award of the American Academy of Neurology in 2017. She authored and co-authored many papers and book chapters about ALS and CMT, such as Epidemiology of ALS and Clinical Features of ALS in Africa. Aqdas Kazi  MBBS, MRCP, CCST (Palliative Medicine), is a consultant in Palliative Medicine at Shifa International Hospital, Islamabad. After MRCP and completion of four years of Specialized Registrar training, she received the Certificate of Completion of Specialized Training in Palliative Medicine from the Royal College of the Physicians of the UK.  After working at Singapore General Hospital with the hospital based palliative care team, she established the Palliative Care Unit at Shifa and is the lead for Home Based Palliative care. She teaches medical staff and has been an active advocate for Palliative Care at the national level. Satish Khadilkar  is one of the first few Indian neurologists to pursue the subspecialty of neuromuscular disorders, nationally and internationally. He has been involved with a new clinical sign, sarcoglycanopathies and dysferlinopathies and the gene in calpainopahties. He has over 130 publications to his credit and has written six and edited one book on neurology. He has been trustee and secretary of the Muscular Dystrophy Society and National Vice President of Multiple Sclerosis Society of India. He was the

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president of the Indian Academy of Neurology in 2018 and is the treasurer of Asian Oceanian Myology Center, where he represents India. Seung Hyun Kim  MD, PhD is Professor of Neurology and Director of ALS Clinic and Cell Therapy Center at Hanyang University Medical Center, Seoul. He earned his M.D. degree in medicine and Ph.D. in neuroanatomy from Hanyang University. He has pursued the field of ALS and neurodegenerative disorders. He is conducting translational research in the development of personalized medicine. He received the Secret of Life Award, Award from Ministry of Science, ICT and Future Planning. He serves as a member of the National Academy of Medicine of Korea and Editorial member of Molecular Neurodegeneration. Jerome E. Kurent  MD, MPH, is Professor of Neurology and Medicine at the Medical University of South Carolina and director of the ALS Multidisciplinary Clinic at the Ralph H. Johnson Veterans Affairs Medical Center. He completed residencies in Neurology and Internal Medicine at the Johns Hopkins Hospital, followed by fellowships in neuromuscular diseases and electromyography at the National Institutes of Health. He was a founding member of the MUSC ALS Multidisciplinary Clinic and served on the National Hospice and Palliative Care Organization ALS Work Group. Kurent has served as chair of the American Academy of Neurology Ethics Section, and the AAN Pain and Palliative Care Section. Stela Lefter  MD, is a consultant neurologist with subspecialist interest in neuromuscular disorders. She received her specialist training in Neurology from the Royal College of Physicians of Ireland. She trained in neuromuscular diseases at the National Neuroscience Centres in Dublin and Cork, Ireland, and MRC Centre for Neuromuscular Diseases, National Hospital for Neurology and Neurosurgery, Queen Square, London. Lefter was conferred with an M.D. degree in 2015 for her thesis ‘A Population-Based Epidemiologic Study of Adult Neuromuscular Disease in the Republic of Ireland’. Her specialist research interests include muscle diseases, ALS, and peripheral neuropathies. Tauana  Bernardes  Leoni  MD, is a neurologist in the Department of Neurology at the School of Medical Sciences at the University of Campinas (UNICAMP), Campinas, Brazil. She supervises the clinical care of patients

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at the ALS outpatient clinic at UNICAMP hospital. Leoni is pursuing her PhD working in a research project devoted to characterizing the genotypes, phenotypes and imaging signatures of familial ALS in Brazil. She is a fellow of the Brazilian Academy of Neurology. Wojciech  Leppert  is involved in the palliative care of patients at out– patient clinic, home hospice, and in consultations of patients in different units in hospitals. He has experience in oncology and his main area of research is pain and quality of life of patients and families in supportive and palliative care. He is Editor-in-Chief of an international journal Palliative Medicine in Practice, was elected in 2018 as a President of the Polish Association for Palliative Care, and was appointed in 2019 as National Consultant in palliative medicine in Poland to the Ministry of Health. Westerly Luth  is a research associate at the University of Alberta, working on projects under Wendy Johnston’s qualitative research program. Her background is in psychology and public health. Susan  Mathers is a neurologist at Monash Health, Adjunct Senior Lecturer, School of Clinical Sciences, Monash University and Clinical Director of Neurology at Calvary Health Care Bethlehem, Melbourne. Her clinical and research interests focus on the management of progressive neurological diseases and models of care. She is a member of the scientific committee of the Motor Neurone Disease Research Institute of Australia, the Fight MND CURE Sub-Committee and a founding member of the Australian Motor Neurone Disease Registry and Victorian MND research tissue bank. Christopher McDermott  received his medical degree at the University in Leeds. He undertook the Wellcome Trust Research Training PhD Fellowship and completed his Specialist Training in Neurology at the University of Sheffield, becoming a Consultant Neurologist in 2006. McDermott is now the Professor of Translational Neurology at SITraN and a Consultant Neurologist at the Sheffield Teaching Hospitals Foundation NHS Trust, regularly undertaking specialist MND and neuromuscular clinics in Sheffield. He aims to develop the evidence base for delivering supportive and symptomatic care for patients living with MND. He is chair of the NIHR UK MND Clinical Studies Group.

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NOTES ON CONTRIBUTORS

Hiroshi  Mitsumoto MD, DSc, is the Wesley J.  Howe Professor of Neurology at Columbia University at The Neurological Institute of New  York and New  York-Presbyterian Hospital/Columbia University Medical Center. Mitsumoto has devoted his clinical and research effort to the investigation of ALS in both animal models and clinical trials in patients with ALS.  He has written and lectured extensively on the topic of ALS.  He served as Chair of the ALSA Medical Advisory Board until 1999 and is now a member of the MDA Medical Advisory Board, ALS CARE Board of Directors, and Neurology editorial board. Amina Nasri  is Assistant Professor of Neurology in the Department of Neurology, Razi Hospital. She is investigator in the Clinical Investigation Centre (CIC), member of the Tunisian Neurology Society since 2011 and fellow of the European Board of Neurology since 2015. She is member of the Movement Disorder Society since 2014. She won the International Scholarship Award of the American Academy of Neurology in 2020. She authored and co-authored many original papers or book chapters about movement disorder and Alzheimer disease as well as ALS. D. V. Nevzorova  graduated from Medical University in Ryazan in 1998. She entered the First Moscow Hospice in 2004 as head of department and in 2012 she was appointed to the position of Chief Medical Officer. In 2015 she became the Head of Federal Research and Clinical Center for Palliative Care at Sechenov First Moscow State Medical University. She is the chief specialist in palliative medicine in Russia and co-­author of Clinical Guidelines on Chronic Pain in Palliative Care Patients. Asfandyar Khan Niazi  MBBS, MRCP, MPH, is the academic chief resident (PGY 5) in the Department of Neurology at Shifa International Hospital, Islamabad, Pakistan. He graduated from Shifa College of Medicine in 2014. He holds membership of the Royal College of Physicians (MRCP) of the UK and a Specialty Certificate Examination in neurology. He also has a background in public health with an MPH from the University of London. He has a keen interest in neurodegenerative and neuroinflammatory diseases. Mieko  Ogino MD, PhD, MMA, is board certified Neurologist and board-certified home care physician. She was a post-doctoral research fellow at Columbia University for four years, and was awarded a PhD degree from Kitasato University in 1994; she received the Master of Medical

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Administration from Tokyo Medical and Dental University in 2008. She also finished a course at the Center for Biomedical Ethics and Law (CBEL) in Tokyo University 2005 and became a specialist in clinical ethics. She is the advocate for palliative care for non-cancer patients, especially neurological diseases. She is a director of various academic societies and member of several national associations. Yomi  Ogun BSc (Hons); MBChB; MPH (London), is Professor of Internal Medicine/Neurology and Consultant Physician/Neurologist at Lagos State University College of Medicine Teaching Hospital. With over 90 publications, he is a leading practicing neurologist in Nigeria and an authority on NeuroHIV, Stroke and Neurophysiology (EMG/ NCS). Ogun is a Fellow of the Association of British-Council Fellows and the Royal Society of Tropical Medicine/Hygiene (U.K), and has been a member of the AAN-International Subcommittee 2019 and the WHO Stroke Rehabilitation-Program Interventions 2019, President of the African Academy of Neurology (2017–2019), President of the NSO, and President of NSNS/PANS. Kiwook  Oh  MD, PhD, is an associate professor in the Department of Neurology, College of Medicine, Hanyang University, Seoul, Korea. He received his M.D. and Ph.D. degrees from Hanyang University. Since his early career, he is committed to patients with neurodegenerative diseases. His work focuses specifically on clinical genetics and clinical trials of ALS and neurodegenerative disease. His current project is ‘Genetic architecture and clinical characteristics of Korean patients with motor neuron disease’. David Oliver  has recently retired from his full-time position as Consultant Physician in Palliative Medicine at the Wisdom Hospice in Rochester, Kent and is an Honorary Professor at the Tizard Centre at the University of Kent. He has lectured and published widely on neurological palliative care, particularly on the care of people with motor neuron disease. He was the Chair for the UK National Institute for Health and Care Excellence Guidelines on MND, released in February 2016. He is principal editor of “Palliative Care of Amyotrophic Lateral Sclerosis— from diagnosis to bereavement”. Evy Reviers  is the daughter of an ALS patient, which is her motivation to serve as a representative of pALS at the national and international level. She is CEO of ALS Liga Belgium, focusing on stimulating and financing

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scientific research on ALS, contacts with ALS researchers, collaborations with university hospitals, and defending the rights of pALS at governmental institutions and agencies. As Chairperson of the European Organization for Professionals and Patients with ALS (EUpALS), she is particularly involved in regulatory aspects of ALS clinical trials and advocates the same rights for access to trials and future medicines for all pALS worldwide. Ildefonso Rodriguez-Leyva  MD, MSc, PhD, is head of the Neurology Program of the Faculty of Medicine of the Autonomous University of San Luis Potosí and is the Head of the Neurology Service of the Central Hospital “Dr. Ignacio Morones Prieto” from San Luis Potosi, SLP, Mexico. He has dedicated himself to educate physicians and improve the quality of Neurology in his country, by advancing the relationship of Mexican Neurology with the American Academy of Neurology, American Neurological Association, American Epilepsy Society, Movement Disorders Society, and the World Federation of Neurology. Roman  Rolke  is Director of the Department of Palliative Medicine at RWTH Aachen University, Germany, since 2014. He is co-speaker of the Neuropalliative Working Group of the German Neurological Society and co-speaker of all physicians of the German Palliative Care Association. His research interests include assessment of pain profiles using quantitative sensory testing and late-stage neurological disorders. He is editor of several books on pain and palliative medicine. Rolke is Associate Editor of the German Journal of Palliative Medicine. Ikram Sghaier  has a BSc degree in analytical and experimental biology, M.Sc. degree in microbiology and molecular epidemiology, Specialist in immuno-genetics and virology. She won the Award for best participation in 2012 and 2015 from “STGE” during her PhD. She is Post-doc in the neuro-genetics laboratory, neurology department in RAZI Hospital Tunisia and the Clinical investigation centre (CIC) and is focusing in Amyotrophic lateral sclerosis disease (genetic background and atypical clinical features) Bugyeong Son  RN, is a nurse coordinator at the Cell Therapy Center, Hanyang University Medical Center, Seoul, Korea. She earned her bachelor’s degree in science of nursing from Hanyang University. She has clinical nursing experience in the oncology department and has been involved with ALS/MND since joining Cell Therapy Center. She

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became a Director of International Cooperation in Korean ALS Association in 2019 and is now a second-year master’s student at Hanyang University. Ludo Van Den Bosch  is a scientist investigating the molecular mechanisms involved in different neurodegenerative diseases, including ALS. In addition, he develops new therapeutic strategies for these diseases. He is full professor of Neuroscience at the University of Leuven and group leader at the VIB-Center for Brain & Disease Research. He is head of the Laboratory of Neurobiology and scientific founder of Augustine Therapeutics, a spin-off of VIB developing therapeutic strategies for neurodegenerative disorders. Philip Van Damme  is a neurologist at the University Hospital Leuven. During his neurology training, he undertook a PhD on the role of excitotoxicity in ALS. Afterwards he continued to focus on the neuromuscular disorder ALS. He is Professor of Neuroscience at the University of Leuven and is currently directing the Neuromuscular Reference Center, which coordinates the care of ALS patients. His research activities focus on translational ALS research including fundamental studies to understand the causes and disease mechanisms of ALS, clinical studies on biomarkers of the disease and prodromal disease stages, and clinical trials with novel treatments for ALS. Ludo Vanopdenbosch  is a private neurologist with subspecialty interests in neuro-oncology and multiple sclerosis. He is also director of palliative care and head of the ethics committee at AZ Sint Jan Brugge. His research interest is palliative care in neurology. At present he is co-chair of the scientific panel on palliative care of the European Academy of neurology. He is guest professor at the University of Leuven and the Free University of Brussels. Simone  Veronese  MD, PhD is a consultant in palliative care, head of research at Fondazione FARO, Turin, Italy. He is a member of the Italian Society for Palliative Care (SICP), of the Group of Study for Bioethics and Palliative Care of the Italian Society of Neurology (SIN), and of the Reference Group for Neurology of the European Association of Palliative Care (EAPC). He is the author of several articles on the role of palliative care in neurodegenerative conditions, and on quality of life and outcome measurements.

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NOTES ON CONTRIBUTORS

M. N. Zakharova  graduated from Sechenov Medical Institute in 1979. She started to work in the Research Center of Neurology as a resident and now she is head of the department. She is a professor on the Medical Faculty of Moscow State University and author of more than 200 articles and book chapters. She is co-author of the Clinical Guidelines on Multiple Sclerosis and Amyotrophic Lateral Sclerosis.

List of Figures

Fig. 3.1

Kaplan-Meier curve of patients seen at the University Hospitals Leuven before 2009 (n = 474) and after 2009 (n = 726)53 Fig. 5.1 CALS sites. (Adapted from Zinman et al. 2013) 84 Fig. 9.1 Management structure of the ALS/MND services in Ireland 135 Fig. 22.1 USA Annual ALS Research Budgets 2012–2020. Annual ALS Research Budgets for Fiscal Years 2012–2020 for National Institutes of Health (NIH), Department of Defense ALS Research Program (DoD ALSRP), Center for Disease Control and Prevention—Agency for Toxic Substances Disease Registry National Amyotrophic Lateral Sclerosis Registry (CDC ALS Registry), Department of Veterans Affairs (VA) and Amyotrophic Lateral Sclerosis Association (ALSA). Original source material available at NIH = https://report.nih.gov/ categorical_spending.aspx; DoD ALSRP = http://cdmrp.army. mil/about/fundinghistory; CDC ALS Registry = https:// www.atsdr.cdc.gov/features/alsregistryanniversary/index. html; VA = https://cdmrp.army.mil/alsrp/pdfs/ALSRP%20 Strategic%20Plan.pdf; ALSA = http://www.alsa.org/ about-us/financial-information.html306

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List of Tables

Table 1.1 Table 1.2 Table 1.3 Table 1.4 Table 1.5 Table 2.1 Table 4.1 Table 4.2 Table 7.1 Table 20.1 Table 22.1 Table 23.1 Table 23.2 Table 23.3 Table 23.4

Conditions that can mimic ALS/MND Symptom management Selected ethical issues and controversies Triggers for initiating discussion about end-of-life issues in ALS/MND Country characteristics Proportions in each place of death (percent) 2017–18 Phenotypic characterization of Brazilian patients with ALS Items provided by Public Healthcare in Brazil for patients with ALS Overview of palliative care and hospice services across Germany Multidisciplinary team disease management in Tunisia ALS deaths per year with location of death Incidence and prevalence of ALS/MND Support for caregivers of patients with ALS/MND Access to multidisciplinary clinics Access to palliative care/hospice

5 10 12 14 22 34 67 70 113 270 307 330 336 339 340

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CHAPTER 1

Introduction to Public Policy of ALS/MND Jerome E. Kurent, David Oliver, and Robert H. Blank

Abstract  This chapter outlines the framework and goals of this cross-­ national study of amyotrophic lateral sclerosis/motor neuron disease (ALS/MND) policy. It also describes the key features of ALS/MND and discusses criteria and associated challenges in making the diagnosis and the importance of excluding ALS/MND mimics. Epidemiology, genetics and possible environmental risk factors for ALS/MND are reviewed. Management of symptoms, challenges confronting caregivers, including access to palliative care and hospice during the end-of-life, and the broad range of ethical issues surrounding ALS/MND care are highlighted. This chapter examines the often-ignored public policy context and the importance of cultural and religious factors in understanding policy differences which exist across countries. Finally, this chapter introduces the countries

J. E. Kurent Medical University of South Carolina, Charleston, SC, USA e-mail: [email protected] D. Oliver University of Kent, Canterbury, UK e-mail: [email protected] R. H. Blank (*) University of Canterbury, Christchurch, New Zealand e-mail: [email protected] © The Author(s) 2021 R. H. Blank et al. (eds.), Public Policy in ALS/MND Care, https://doi.org/10.1007/978-981-15-5840-5_1

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selected for this study and summarizes the key topics of importance the authors were asked to address in their chapters. Keywords  ALS • MND • Public policy • Cross-national studies • Multidisciplinary teams • Palliative care • End-of-life decisions

Introduction Incurable progressive neurological disorders cause immense pain and suffering for their victims and their families. The associated huge economic and indirect costs to society are often difficult to calculate. A rapidly growing aging population in many regions of the world is strongly associated with the increased incidence of neurodegenerative disease and has major public policy implications. Amyotrophic lateral sclerosis/motor neuron disease (ALS/MND) may be the prime example of a devastating rapidly progressive neurodegenerative disease for which there is no cure or significant disease-modifying therapy. Although there are three approved drugs used for the treatment of ALS/MND, their benefits are limited, and most other treatment options are limited primarily to symptom management. There is a clear need for effective public policy and research focused on ensuring optimal clinical care of patients with ALS/MND and provision of adequate supportive services. Increased research funding focused on an enhanced understanding of the etiology(ies) and pathophysiology of ALS/MND and mechanisms of motor neuron cell death is expected to lead to development of additional disease-modifying agents and ultimately to a cure. There is also the potential that insights gained from the study of ALS/MND may provide clues to other enigmatic neurodegenerative diseases, including dementia, that plague our societies. A primary goal of this book is to develop a compendium of public policy summaries representative of many different countries across the globe. It discusses a range of ALS/MND policy elements and perspectives while providing a framework for understanding ALS/MND as it affects patients and their families, professional caregivers and researchers. The book should be of interest to those involved in health care policy and public health as well as for ALS clinicians including neurologists, nurses, nurse practitioners, allied health professionals and physicians’ assistants involved in the complex range of issues related to ALS/MND. Additional stakeholders who should find this book of interest include social workers, ALS clinic coordinators and administrators and members of ALS and MND

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private foundations and public agencies dedicated to the optimum treatment of patients with ALS/MND—including the goal of its ultimate defeat. The book may also serve as a useful reference for organizations providing durable medical equipment such as wheelchairs, communication devices, beds and other assistive equipment utilized in the management of patients with progressive disability.

What Is ALS/MND? ALS is a progressive fatal neuromuscular disease first described by Charcot in 1869 which primarily affects spinal cord and brainstem motor neurons and the upper motor neuron system. ALS may be regarded as a syndrome rather than a specific disease entity. There is increasing evidence of wider neuronal involvement, including the frontal lobes, and cortical and subcortical regions (Westeneng et  al. 2016). ALS is also known as Lou Gehrig’s disease in the United States, named after the famous major league baseball player who succumbed to this illness in 1941, whereas in the United Kingdom, motor neuron disease is used to designate ALS. Within the classification ICD-9 (code 335.2), the term motor neuron disease is also indistinguishable from ALS.  It has been suggested that the term motor neuron diseases be used to include both ALS and its clinical subtypes. Thus, ALS/MND as used here encompasses: • ALS/MND, with both upper and lower motor neuron involvement, leading to a mixed picture of weakness associated with spasticity and flaccidity, muscle wasting, fasciculation and extensor plantar responses; average longevity three to five years; more than 90 percent of people with limb onset develop bulbar symptoms; • Progressive bulbar palsy affects about 20 percent of patients in which there is involvement of the bulbar motor neurons, affecting speech and swallowing; • Progressive muscular atrophy (PMA) affects about 5 percent, with predominantly lower motor neuron involvement leading to muscular weakness and wasting, particularly of the legs and arms. The prognosis is longer and may be five to ten years; • Primary lateral sclerosis (PLS) which affects 1–2 percent with predominantly upper motor neuron involvement, including spasticity,

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stiffness, increased deep tendon reflexes and extensor plantar response. It has a longer prognosis often greater than ten years The most common clinical presentation of ALS/MND is spinal-onset and involves slowly progressive painless weakness and atrophy of a distal upper or lower extremity. Weakness typically progresses to involve the contralateral limb and then to other areas of the body including bulbar and respiratory muscles. Rarely—less than 5 percent—do patients first present with respiratory failure that requires ventilator support. The average age of onset is 55 to 57 years, with a male to female ratio of 1.7:1, except 1:1 having onset after 65 to 70 years of age. Death typically occurs within three to five years from respiratory muscle failure, although 25 percent of patients survive for five years and 10 percent are alive at ten years (Shaw et al. 2014). Frontotemporal dementia (FTD) occurs in up to 15 percent of patients (McKhann et al. 2001). More subtle frontal lobe dysfunction may occur in another 20 to 25 percent of patients (Lomen-Hoerth et al. 2003; Strong et al. 2009; Phukan 2012). There are patients with FTD who later develop ALS/MND with a spectrum from pure ALS to pure FTD—often related to the C9orf72 genetic abnormality (Couratier et  al. 2017). An estimated 90 to 95 percent of patients have sporadic ALS (sALS) which occurs in the absence of a clear family history. Five to 10 percent of ALS patients have familial ALS (fALS) usually inherited as a Mendelian autosomal dominant gene. Reduced penetrance is not uncommon.

Making the Diagnosis of ALS/MND: A Diagnosis of Exclusion The neurologist must take a careful history and perform a meticulous neurological examination to determine if an alternative cause of the patient’s symptoms can be identified. Depending on localizing signs and symptoms, MRI imaging of the spine is often necessary to rule out structural lesions, such as cervical or lumbar stenosis, herniated disc with foraminal encroachment and spinal cord compression, meningioma and other spinal cord pathology. Although there are no specific biomarkers currently available to confirm the diagnosis or to monitor the clinical course of ALS/MND, efforts are underway to identify biomarkers.

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Table 1.1  Conditions that can mimic ALS/MND Spinal cord pathology that causes spinal cord and/or nerve root compression (myeloradiculopathy) includes but is not limited to cervical spondylosis and meningioma Autoimmune neuropathies—including multifocal motor neuropathy Spinobulbar muscular atrophy (Kennedy’s disease) Multiple sclerosis Hereditary spastic paraplegia Benign fasciculation syndrome Myopathies—inclusion body myositis Diabetic amyotrophy Thyrotoxicosis Hyperparathyroidism

As illustrated in Table 1.1, there are many conditions that can mimic ALS/MND. A second independent opinion from a neuromuscular specialist having special expertise in ALS/MND is often requested by the first neurologist suspecting ALS/MND in order to confirm the diagnosis of what many consider to be a “death sentence.” Muscle biopsy and spinal fluid examination are not considered necessary for routine evaluation of patients suspected of having ALS/MND, but they may be helpful in diagnosing a suspected alternative condition or ALS mimic. Criteria have been developed to assist with the diagnosis and management of ALS. These include the modified El Escorial criteria (Brooks et al. 2000), which are particularly relevant when considering clinical drug trials. The criteria suggest that for a diagnosis of ALS/MND, there should be progressive upper and lower motor neuron deficits in at least one limb or region of the human body (meeting the revised El Escorial criteria for possible ALS) or lower motor neuron deficits as defined by clinical examination (one region) and/or by EMG in two body regions (defined as bulbar, cervical, thoracic, lumbosacral). There must be progressive changes, fasciculations and near normal motor nerve conduction and no sensory abnormalities. There should be no abnormalities of the sensory nervous system, no impairment of the visual or autonomic nervous system and no sphincter involvement. The Awaji criteria were subsequently developed and are based on the expanded role of the electrophysiological diagnosis of ALS/MND (Chen et al. 2010; Costa et al. 2012). Electromyography is a critical component

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of diagnosing ALS/MND. Diffuse denervation should be present in three different anatomical regions to meet electrophysiological criteria for the diagnosis of ALS/MND. Fibrillations and positive waves consistent with active denervation are typically present and are usually seen in association with high amplitude, prolonged duration motor unit potentials consistent with chronic denervation/re-innervation. Fasciculation potentials are often present. It is imperative that ALS/MND mimics have been ruled out.

Epidemiology of ALS/MND The incidence of ALS/MND across the world is unclear. A systematic review suggests that the incidence in Europe is 2–3/100,000 with a prevalence of 5–7/100,000 population (Chio et al. 2013), while the incidence of ALS in the United States is approximately 3–5/100,000. It is unclear if the differences across countries relate to the design of studies, the ability of patients to receive medical attention or differences in defining ALS/MND. Although considered a rare disease, the incidence of ALS/MND is approximately one-half that of multiple sclerosis (MS). However, public perception and general awareness of MS is much greater than that of ALS/MND primarily due to the marked contrast in life expectancy for victims of these two disorders. Although patients with MS face a reduction in life expectancy of seven to twelve years (Magyari and Sorensen 2019), most patients with ALS/MND will not survive more than three to five years after diagnosis. The incidence of ALS/MND in the non-Caucasian population and individuals of mixed ethnicity is considered less than whites of European ancestry. In the Western Pacific the incidence of ALS among the indigenous Chamorros in Guam had occurred at rates 50 to 100 times that noted elsewhere around the world (Armon 2013). ALS often co-existed with Parkinson-dementia complex. The incidence of Guamanian ALS has dramatically dropped since World War II, and it is suspected that dietary toxins present in cycad seed, which were used as a primary source of dietary flour, along with a possible genetic predisposition, may have been at least in part responsible for this phenomenon. Genetic susceptibility may have contributed to an increased incidence of ALS in the Kii Peninsula of Japan, which also represents a well-known, but poorly understood, ALS cluster.

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Genetics of ALS/MND The genetics of ALS/MND has become increasingly complex. The first ALS gene mutation—SOD1—was reported in 1993 (Rosen et al. 1993). There are now more than twenty different genes known to cause ALS. The majority of familial ALS is transmitted as a Mendelian autosomal dominant gene, but penetrance may be incomplete. The most common genes are: • SOD1—accounting for 10–20 percent of fALS and 1 percent of sALS • C9orf72 hexanucleotide repeat—accounting for 40 percent of fALS in many countries, but less than 10 percent in Asia, found in 10–20 percent of sporadic ALS in Europe • TDP-43—accounting for 4 percent of fALS and less than 1 percent of sALS • FUS/TLS—accounting for 4 percent of fALS and more rare in sALS • Ataxin 2—accounting for 4 percent of fALS and 1 percent of sALS • VCP—accounting for 1–2 percent of fALS (Corcia et al. 2017) Reviews have described in detail the rapidly evolving body of knowledge related to the genetics of ALS/MND and their contribution to advancing our understanding of the underlying basis for this disorder and means to develop effective therapies (Andersen and Al-Chalabi 2011; Brown and Al-Chalabi 2017). The investigation of these genetic mutations is providing some insights into mechanisms of motor neuron cell damage and death. Until recently, numerous clinical trials with humans affected with ALS/MND have not been able to duplicate positive results reported in animal studies (Benatar et al. 2009). However, the development of gene-specific therapies for ALS/MND may indeed be realized in the case of the SOD1 mutant gene and C9orf72. The development of anti-­ sense oligonucleotides is well underway along with early-stage clinical trials for individuals having the SOD1 genetic variant and C9orf72 (Ly and Miller 2018; Miller et al. 2020). SOD1 suppression with adeno-associated virus and microRNA was also recently reported (Mueller et al. 2020). There is the underlying assumption that patients with sALS have a genetic predisposition for developing ALS/MND. The presumed genetic predisposition alone is considered insufficient, but in conjunction with

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other factors including environmental influences, it can trigger a process resulting in clinical ALS/MND. It has been suggested that a six-step process occurring over the life of an individual may converge with a genetic predisposition to initiate the cascade of motor neuron damage and cell death, resulting in ALS/MND (Al-Chalabi et al. 2014; Chio et al. 2018). Identical twin studies have failed to demonstrate an increased risk of developing ALS in the unaffected sibling (Al Chalabi et al. 2010; Xi et al. 2014; Tarr et al. 2019), perhaps supporting the suspected role of environmental factors and epigenetics.

Environmental Risk Factors The suspected role of environmental factors as they relate to genetics in ALS has been discussed in detail (Al-Chalabi and Hardiman 2013). Numerous toxins and other insults as well as nutritional deficiencies have been considered. The role of physical trauma and emotional stress has also been studied, but without demonstrating a clear relationship to causality. More recent observations related to a suspected increased risk of ALS and other neurodegenerative diseases in US National Football League (NFL) professional athletes have been highlighted. The possible role of chronic traumatic encephalopathy (CTE) in a subgroup of patients with ALS has been suggested (McKee et al. 2010), although other reports have questioned this relationship (Bedlack et al. 2011; Armon and Miller 2011). Toxins and other environmental agents which have been investigated include smoking, alcohol, heavy metals like lead and mercury, pesticides and electric shock. Smoking has been associated with ALS/MND risk in several studies, although its precise role in susceptibility has not been defined. Inhalation of other environmental toxins associated with urban pollution is also being investigated (Malek et al. 2013; Seelen et al. 2017). There is also renewed interest in toxins associated with cyanobacteria, which have ubiquitous presence in the environment. Viral infections including reverse transcriptase agents have been studied, but without definitive proof of causality. Patients with HIV/AIDS have developed ALS, but their neurological disability has not responded to antiviral therapy In the United States, ALS has been declared a military service-­connected disability based on several epidemiological studies (Horner et  al. 2003; Weisskopf et al. 2005), suggesting a two-fold increase in risk for developing ALS by deployed veterans. An increased risk was first described for veterans deployed to Iraq, and subsequently for those involved in earlier

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conflicts and wars dating back to World War II. Numerous factors related to military service have been considered, but without demonstrating a direct causal link to ALS.  These factors include burning oil fields, as in Iraq, multiple immunizations, concussion and other physical and emotional stressors, as well as nerve toxin antidotes, such as pyridostigmine. Italian soccer players have also experienced a significantly increased risk of developing ALS, but for unknown reasons. Occasional clustering of patients with ALS/MND has been reported, suggesting possible common environmental exposures, but with inconclusive findings.

Management of Symptoms Multidisciplinary ALS clinics are considered the gold standard for providing comprehensive care (NICE 2016; Miller et al. 2009) and are widely accessible through most of North America, the United Kingdom, Europe and many countries around the globe. Their implementation has been associated with improved quality of life and possibly extension of the natural history of ALS/MND (Aridegbe et al. 2013; Rooney et al. 2015). The ALS Functional Rating Scale-Revised (ALS-FRS-R) is a tool routinely utilized in multidisciplinary clinics to monitor overall clinical status of the patient and is a reliable measure of clinical progression and loss of function (Cedarbaum et al. 1999). Numerous excellent resources are available to guide the clinical management of patients with ALS/MND (Miller et al. 1999; Miller et al. 2009; Bedlack and Mitsumoto 2013). Most patients with ALS/MND will die of respiratory failure secondary to weakness and atrophy of diaphragmatic and accessory muscles of respiration. Patients will experience a wide range of disabling symptoms over the course of their illness including dyspnea, weakness and atrophy, muscle cramps, dysarthria, dysphagia, weight loss, pathological laughter and crying (pseudobulbar affect), drooling, pain, sleep disturbance and constipation (see Table 1.2). Multidisciplinary ALS clinics provide a wide range of professional expertise required to assist with management of these symptoms while providing comprehensive care for the patient and support for family caregivers.

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Table 1.2  Symptom management Symptom

Management

Pain

Muscle spasm Musculoskeletal Skin pressure

Cramps

Fasciculations Spastic muscles

Spasticity

Muscle spasm

Sialorrhea

Reduced swallowing

Thick secretions

Laryngospasm Insomnia

Pseudobulbar affect

Anxiety Respiratory failure Depression Uncontrolled laughter/crying

Dyspnea

Respiratory muscle weakness and respiratory failure

Dysarthria

Speech and language therapy assessment Speech and language therapy and dietitian assessment Frontal lobe dysfunction Frontotemporal dementia Language/loss of empathy/ executive function loss/ memory loss Poor diet/anticholinergic medication side effects Lower esophageal sphincter weakness

Dysphagia Cognitive issues

Constipation Gastroesophageal reflux disease

Muscle relaxants Nonsteroidal anti-inflammatory Analgesics/opioids Quinine sulfate (not available in US) Baclofen Gabapentin Tizanidine Baclofen Tizanidine Gabapentin Physiotherapy Atropine/scopolamine Botulinum toxin injections Radiotherapy to salivary glands N-acetylcysteine Grape fruit juices Nebulized water Sublingual lorazepam Anxiolytics Noninvasive ventilation Antidepressants Amitriptyline, Dextromethorphan/quinidine sulfate Noninvasive ventilation Opioids Tracheostomy ventilation Communication aids Modified consistency of food Consider gastrostomy Psychological assessment Advice and support for caregivers

Fluid and fiber Laxatives Meals while upright H-2 blockers Proton pump inhibitors

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Palliative Care, Hospice and End-of-Life Care As there is no curative treatment for ALS/MND, the approach is often palliative. The World Health Organization (WHO) defines palliative care as “the total active care of patients whose disease is not responsive to curative treatment. The goal of palliative care is the achievement of the best quality of life for patients and their families.” The involvement of specialist palliative care/hospice care for ALS/MND started first at St Christopher’s Hospice in London, UK, in 1967 and has spread across the world. Many guidelines have recommended palliative care including the American Academy of Neurology Ethics and Humanities Committee Position Statement (Carver 1996) which highlighted the urgency that neurologists understand and apply principles of palliative care in the management of their patients. The American Academy of Neurology Practice Parameter (Miller et al. 2009) and the EFNS Guidelines (Andersen et al. 2012) further supported this approach. A palliative care approach considers the whole patient in the context of their family and caregivers—assessing the physical, psychological, social and spiritual aspects of care. It encompasses a multidisciplinary approach, and it has been recommended that the multidisciplinary team (MDT) for ALS/MND should include palliative care expertise (NICE 2016; Miller et al. 2009; Robert Wood Johnson Foundation 2004).

Ethical Issues in ALS/MND Care Numerous challenging ethical issues often arise while caring for the patient with progressive neurodegenerative diseases, including ALS/ MND. Table 1.3 illustrates some of these issues related to the management of patients with ALS/MND, beginning with communicating the bad news of the recent diagnosis of ALS/MND to a patient. A comprehensive description of the ethical issues and their resolution as they occur in neurology practice has been provided by Bernat (2008). The subject of breaking the news to the patient with newly diagnosed ALS/MND is a matter of compassion and empathy and should include discussion of the possible available treatments, anticipated future needs, avoidances and preferences of the patient. The National Institute for Health and Care Excellence (NICE) Guidance gives clear recommendations (NICE 2016). The newly diagnosed patient may, or may not, suspect the seriousness of his neurological condition at the time of meeting

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Table 1.3 Selected ethical issues and controversies

 •  Breaking bad news   • Abandonment  •  Enrollment in clinical trials  •  Genetic testing of patients  •  Genetic testing of family members  • Use of feeding tube and option to withdraw once initiated  • Use of tracheostomy and mechanical ventilation   • Palliative sedation   • Physician-assisted suicide   • Euthanasia  • Organ donation by living patient with ALS  • Organ donation by deceased patient with ALS  •  “Right to Try” legislation  • Treatment with unproven and potentially dangerous agents  • Charlatans and quacks offering ineffective or unproven therapies  • Role of public policy in addressing these issues

to summarize results of diagnostic testing with his or her neurologist. It is vitally important for the physician to break the bad news in-person and to allow adequate time for the patient to begin to process this life-changing information. Excellent resources are available to help guide this discussion (Johnston et al. 1996; Sloan and Borasio 2014). The expression “Diagnose and Adios” has been used to characterize some neurologists’ interactions with patients and suggests the lack of adequate empathic connection. This suggests that the neurologist may possibly be more intent on making the correct diagnosis than on caring for the patient. This approach is changing as the neurologist provides ongoing care, often as part of a multidisciplinary team (Gursahani 2016; NICE 2016). In the past, physicians sometimes tried to protect the patient from the bad news of a life-limiting diagnosis by using terms such as a “disease of the motor system” or simply delaying the diagnosis. There is no justification for withholding or downplaying the significance of diagnostic information considered essential to prepare for advance planning and for getting one’s personal and business affairs in order.

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The ethical principle of truth-telling requires that patients be provided honest and accurate information related to their illness. Most patients expect full disclosure of facts related to the diagnosis of serious illness. Prognosis and related discussions may be provided over a series of meetings at a pace comfortable to the patient since some patients may be overwhelmed with too much information provided at one time (Seeber et al. 2019). However, it is important to allow these discussions whenever the patient and family wish to facilitate discussion and to plan for the future (NICE 2016). The responses of patients with newly diagnosed ALS/ MND can be variable (Johnston et  al. 1996; Sloan and Borasio 2014). Some patients have a relatively positive response, “At least I know what I have,” while others can express feelings of despair. There is a delicate balance between the neurologist providing immediate and full disclosure and communicating in a caring and empathic manner. Communication should be tailored to the unique needs of the patient to the extent this can be determined. Cultures vary to the extent to which critical information is expected to be communicated either directly to the patient, or sometimes preferably to family members. Many patients explore the Internet to seek out information related to their symptoms and suspected diagnosis. It is usually helpful to ask the patient what he/she understands about their condition. Most patients have little knowledge about ALS/MND, although this is changing with the increased use of the Internet. A blunt approach used to provide the diagnosis in an abrupt manner is strongly discouraged and can be devastating to the patient and family. It is also reasonable to leave some room for hope, although this may be challenging. Clinical trials may offer optimism for some patients. Medical paternalism, in which the patient is “protected” from bad news, is no longer accepted in most Western cultures. A direct and forthright discussion with the patient is expected. However, some cultures around the world expect that unfavorable information pertaining to a serious diagnosis be provided to family members of the patient rather than to the patient. These cultural norms should be respected by the physician and should be known in advance of the discussion if possible. Patients with ALS have sometimes expressed a sense of physical or emotional abandonment by their physicians as their illness progressed. Non-­ abandonment of the patient is a key ethical obligation shared by all professionals involved in the care of patients with ALS/MND. Abandonment of the patient by a physician can be either physical or emotional. Following the diagnosis of ALS/MND, professional caregivers including physicians

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Table 1.4  Triggers for initiating discussion about end-of-life issues in ALS/MND  • The patient or family asks, or “opens the door,” for end-of-life information and/or possible interventions  •  Severe psychological and/or social or spiritual distress or suffering  •  Pain or other symptoms requiring higher than normal dosages of medications  •  Dysphagia requiring a feeding tube  • Dyspnea or symptoms of hypoventilation, usually with reduced forced vital capacity of 50 percent or less  •  Loss of function in two body regions (bulbar, arms or legs) Modified from Robert Wood Johnson Foundation (2004)

may feel uncomfortable in following up the patient with an incurable disease. Increasingly, the ongoing care is shared within a multidisciplinary team, which shares the load and allows all aspects of care to be considered, often with an improvement of quality and even length of life (Aridegbe et al. 2013). Professional caregivers may have a basic discomfort with death and dying, including fear of death, a sense of failure as well as challenges in confronting one’s own mortality. However, there remains an obligation to discuss end-of-life care issues with the patient having advanced ALS/ MND including the need for advance care planning. Table  1.4 lists six triggers for initiating a discussion about end-of-life care decision-making for the patient with ALS. Clinical Trials ALS/MND clinical trials offer hope for patients, and many are eager to participate. Clinical trial participation should be strongly encouraged. Although most patients appear to fully understand that participation in clinical trials will most likely not be of direct benefit to them, it is important that they have this clear understanding prior to enrollment in the interest of truth-telling and informed consent. Genetic Testing The genetics of ALS/MND have provided critical insights into molecular mechanisms of motor neuron cell damage and death and offer hope that meaningful therapies focused on specific gene defects can be developed. Availability of genetic testing for ALS/MND varies greatly around the world. There are numerous medical-ethical dilemmas arising from the availability of genetic testing for ALS/MND.  Continued acquisition of

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new knowledge related to understanding and ultimately curing ALS/ MND will depend to a great extent on identifying additional genes. A recommendation for routine genetic testing of patients with sporadic ALS has been made, but this raises the challenging issue of the testing of unaffected individuals who are at potential risk of developing ALS/ MND. There also may be issues of payment by insurance companies and restricted resources and availability of genetic counseling and testing in many parts of the world. Genetic testing for clinically unaffected family members at-risk and related to a patient with clinical ALS/MND having a strong family history has been a subject of discussion. Testing of individuals at-risk for developing ALS/MND can provide the opportunity to arrange for family planning in addition to making other key decisions involving employment and the acquisition of medical and life insurance. Genetic counseling prior to and following testing is obligatory whether the individual tests positive or negative for the gene. It has been questioned whether there is an ethical obligation to disclose positive results of gene testing to other family members even though they are not actively participating. Clinically unaffected individuals, although not suspecting that they might be carrying a mutant gene, could potentially benefit from this information. However, even if legislation exists to protect individuals having a genetic mutation, discrimination by insurance companies and employers might still occur, posing serious implications for the economic well-being of clinically unaffected patients who test positive for a deleterious ALS/MND gene. Withholding and Withdrawal of Care There are many ethical and legal issues at the end of life particularly concerning the withholding and withdrawing of care. In many countries there is no ethical or legal distinction between withholding and withdrawing of care, such as the placement or use of a feeding tube or the use of invasive ventilation. Such interventions can be either withheld altogether, or withdrawn once in place. These decisions are typically at the direction of a patient having decision-making capacity or his/her legal surrogate decision-­maker. In some countries it is not legally permissible to withdraw treatment, such as invasive ventilation, once it has been initiated. These approaches vary by country and often have strong cultural underpinnings, which form the basis for law and public policy. Therefore, careful discussion is necessary before any consideration of these interventions, so that a

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clear decision is made; the implications of the intervention, such as the continued deterioration of the disease after ventilatory support has started, are discussed; and plans for future care, including the possible withdrawal of treatment (NICE 2016; Oliver and Turner 2010), are considered. If withdrawal is not possible within a country, these discussions are even more crucial so that a truly autonomous decision can be made. There is increasing awareness of frontotemporal dementia and related cognitive change which can occur in ALS/MND, and a consideration of mental capacity to make decisions and advance care planning is important. There may be opportunities earlier in the disease progression when the person can make decisions and make their wishes for their future care known. If these are recorded clearly, as advance directives or defining a proxy to make decisions on their behalf, the person’s wishes can be respected. However, it may be difficult to have these discussions, and patients and families may be resistant to looking ahead, but this may be the only opportunity as cognition and communication may be lost in the future (Goldstein 2014). Palliative Sedation and Assisted Dying  At the end of life some patients experience significant distress. The aim of palliative care is to minimize suffering, and with good symptom management, a distressing death is considered rare (Neudert et  al. 2001). However, on some occasions the patient may remain distressed—physically, emotionally or spiritually. In certain circumstances therapeutic/palliative sedation may be necessary. The European Association for Palliative Care framework  has suggested  that “Therapeutic/palliative sedation in the context of palliative medicine is the monitored use of medications intended to induce a state of decreased or absent awareness (unconsciousness) in order to relieve the burden of otherwise intractable suffering in a manner that is ethically acceptable to the patient, family and health-care providers” (Cherny et al. 2009). Morphine and benzodiazepine medications are typically used in a closely monitored clinical environment to sedate in order to relieve suffering. The National Hospice and Palliative Care Organization (2010) has provided guidelines for the implementation of palliative sedation in the rare instance that it may be required. This includes the recommendation that patient caregivers as well as the patient, if capable, participate in a detailed discussion with hospice or palliative care professionals caring for

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the patient. This discussion should include the potential for premature death of the terminally ill patient even though this is considered unlikely. The US Supreme Court has also expressed support for palliative sedation. The Principle of Double Effect justifies the morality of a single act that has the potential of causing two morally opposite effects (Bernat 2008). Although the intent is to relieve suffering, the potential to cause the premature death of the patient is acknowledged. Palliative sedation is ethical and legal in many, but not all, countries and should only be considered in the relatively rare instance when all other measures have failed to control the intractable pain and other symptoms not manageable by usually effective therapies. On occasions this may continue until death, but sometimes the level of sedation can be reduced if the patient remains comfortable. Palliative sedation should not be confused with physician-assisted suicide (PAS) or euthanasia/medical aid in dying. Although there appears to be an increasing acceptance of PAS, this varies considerably by country. The patient desiring PAS must be diagnosed with a terminal illness and is provided a prescription by a participating physician for a lethal dose of one or more medications such as a barbiturate. The patient may choose to take the lethal dose of medication at a time and place of his/her choosing. The primary ethical dilemma focuses on patient autonomy and the right to make decisions concerning the fate of one’s body versus the physician’s duty to cause no harm and to preserve life. Euthanasia occurs when a doctor intentionally kills a person by the administration of drugs at that person’s voluntary and competent request (Radbruch et al. 2016). This has been offered only in limited countries where it is legal and to someone with full capacity and autonomy. Euthanasia will always be controversial, even where legal. As discussed in more detail in country chapters, assisted dying is now available in many countries, with varying legal regulations. Euthanasia and PAS are legal in Belgium, the Netherlands, Luxembourg, Canada, Colombia and the states of Victoria and Western Australia in Australia. In the United States,  PAS is legal in nine states and the District of Columbia. Assisted dying is allowed in Switzerland. Patients with ALS/ MND are often overrepresented in the people receiving assisted dying. In the Netherlands in 2010, 1.8 percent of all deaths were a result of either euthanasia or PAS. Twenty percent of MND patients received an assisted death compared with 5 percent of cancer patients and 0.5 percent of people with heart failure (Maessen et al. 2010).

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Some patients with ALS/MND have expressed an interest in being organ donors after time of death. There is reluctance to accept organs from patients with ALS/MND out of concern that the potential for a transmissible agent being present in tissues represents an unacceptable risk to a would-be donor recipient. Ethical concerns relate to weighing organ recipient’s safety versus depriving patients of potentially life-saving organs, albeit from patients with ALS/MND.  On rare occasions, patients with ALS have petitioned to donate organs while still alive, and it has been reported that following euthanasia, the organs were donated (Bollen et al. 2016a, b). Right to Try The “Right to Try” movement offers the potential for patients having incurable diseases to have access to unlicensed drugs and other therapeutic interventions not presently available. There are ethical concerns related to patient safety versus the desire to allow the patient to exercise his/her free will and self-determination regarding personal choice related to risks and potential benefits of unproven therapies. Again, the following chapters show considerable variation across countries. Not surprisingly, charlatans and “quacks” prey on patients with incurable diseases such as ALS/MND. There is a long history of patients with ALS/MND being taken advantage of by such individuals. Useless and potentially harmful potions and concoctions, having no scientific basis, have been taken by patients at considerable personal risk and economic cost. The violation of ethical principles is obvious, but is very difficult to contain.

Public Policy Context Embedded in many of these ethical concerns are legal and public policy issues. Moreover, funding of ALS/MND research and care must compete for public attention and political support for its share of societal resources, not only with non-health areas but also with more visible causes like cancer and AIDS and even other neurological diseases such as Alzheimer’s disease, Parkinson’s disease and MS. The move of ALS/MND to the policy domain also brings to the forefront political deliberations and divisions and places the resolution of issues in the milieu of interest group politics. Given the high economic, social and personal stakes surrounding A ­ LS/

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MND, conflict is unavoidable because each group has its own demands for attention and resources. As noted earlier, the impact of ALS/MND goes well beyond the health care needs of the person affected. As the impact of ALS/MND progresses, the patient becomes increasingly dependent on others for basic daily care and routine tasks, a physically safe environment and protection from exploitation or abuse. Addressing the diverse medical and social care needs of ALS/MND patients requires the adoption of a multifaceted policy framework and agenda that explicitly acknowledge their complex and unique needs and the impact it has on caregivers and society at large. Public policies related to social service agencies that provide housing and financial and legal services must complement other policies. These include research funding, prevention and risk reduction, symptom management, access to assistive technologies and efficient health care delivery. Although there are many books on ALS/MND, none to date provides a major focus on these areas. This book is offered as a first step in filling this void. Funding policies are critical for research to determine the cause(s) of ALS/MND, how to prevent it, diagnose it early and accurately and how to slow its progression, if not cure it. At present, funding levels for ALS/ MND research are low, even on a per-patient level, as compared to cancer, heart disease and AIDS. Furthermore, long-term services and support are critical for ALS/MND patients. Payment policy for both home and institutional care and strategies to support community living are fundamental for those with late-stage ALS/MND. An increasing proportion of patients is likely to spend some time in long-term care facilities at some point in their life. Critically important to support for those who remain in their homes are services such as caregiver support, respite care centers and, at some stage, palliative and hospice care services. Considerably more resources are needed to better understand the impact of environmental factors on ALS/MND and develop more effective preventive strategies. Although to date the public health/preventive dimension of ALS/MND has been constrained, as more is known about its causes, this will become more relevant. Addressing healthy lifestyle and risk factors where they are known as well as community readiness are important for a population approach to managing the growing burden. Related to this is the need for regulation of the marketing of untested natural supplements and other products for ALS/MND patients. Policies must be put in place to address the challenge of ensuring a competent and adequate workforce, especially for hands-on caregivers,

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such as personal care assistants and home health aides. At present much care is informal by family and friends, but this is changing in many countries. A shift to paid caregivers raises questions as to whether they need to be regulated through licensing or other mechanisms. Here again the comparative approach is valuable in how best to develop compensation mechanisms for family caregivers of patients with chronic incurable illnesses. There is also a need to provide protection from potential exploitation, abuse and neglect. Although there is little evidence of abuse of ALS/ MND patients by formal or informal caregivers, it is a well-documented problem with Alzheimer’s patients and others in long-term care. Basic policy questions relate to what institutional services exist for the care of ALS/MND patients; how, where and by whom these patients are treated; how aggressive and costly the treatment regime is (e.g. what is the availability of intensive care units?); who makes the final decisions as to level of care given; and who pays the escalating costs? What types of hospice operate and what level of palliative care and pain management are accessible to patients with ALS/MND? More specific questions regarding the end of life relate to availability of medical specialists and adequate pain management, palliative care and hospice services. Control of pain, of other symptoms and of psychological, social and spiritual problems is paramount to provide the best possible quality of life for patients and their families. Accompanying the medical dimensions of policy-making at the end of life are the social and legal aspects. In many Western countries, considerable emphasis in recent decades has been directed toward empowerment of the patient or patient autonomy. A wide variety of legal mechanisms have been created toward this end. Prominent among these advance directives (ADs) are the living will and the durable power of attorney for health care. The stated goal of ADs is to return to the individual the ability to control the dying process, by expressing avoidances and preferences often related to life-extending interventions. However, they also include a resource allocation dimension and in most cases are designed to specify limits on continued treatments, but in some instances may include the directive to “do everything possible.” A key policy question is how different countries define and deal with these challenging end-of-life issues.

Cross-cultural Studies The cross-national policy context presented in this book is crucial in comparing how various countries are dealing with these issues and for learning what are the most effective policies to pursue. Although it is risky to

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uncritically apply policies that appear to work in one country to another, cross-national research is useful to generate the evidence necessary to consider the full array of policy options open to decision-makers. Exploring the experiences of their counterparts in other jurisdictions in dealing with similar problems can be invaluable. An examination of international experiences also illuminates both the difficulties faced by and the range of approaches available to policy-makers. Studying the issues surrounding ALS/MND across many country settings can elucidate the commonalities of problems and variables across countries and provide valuable strategies for framing policy. Likewise, cultural factors and social values vary across countries and in some cases are most crucial for ALS/MND policy. Values dominant in the West such as individual rights, personal autonomy, truth-telling and the dependence on technology to fix problems, including death, are not universal, despite what much of the bioethics literature assumes. Moreover, there may be strong cultural and value divisions within each country that are important in understanding policy issues. For instance, religious beliefs are a particularly critical dimension for death-related policies, and perhaps the single most important factor in some countries. Moreover, social structures can be central to the care of the chronically and terminally ill and in setting the boundaries of such care. In many countries extended families and communities still have a central role to play, while in other countries even the nuclear family seems to play a limited role in caregiving.

Countries Selected One of the goals of this book was to expand the scope of the study to include a diverse range of countries, especially low- and middle-income countries that are often neglected. The editors were successful in commissioning chapters from twenty-one countries across the globe. As illustrated in Table 1.5, they span six continents and are representative of large and small, younger and older populations, reflecting wide variations in growth rates and urbanization and a broad range of GDP and economic variables. The health policy of any country is the product of a multitude of factors including the intrinsic social, cultural and political fabric of a country, its political institutions and traditions, the legal system and the characteristics of its health care community. For instance, policy-making authority might be highly centralized or widely dispersed across multiple levels. Moreover, in some countries, unions and/or corporate structures are strong factors in determining social policy and might, in effect, have a veto power over

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Table 1.5  Country characteristics Country

Population

Australia 25,088,636 Belgium 11,562,784 Brazil 212,392,717 Canada 37,279,811 China 1,420,062,022 Germany 82,438,639 India 1,368,737,513 Ireland 4,847,139 Israel 8,424,904 Italy 59,216,525 Japan 126,854,745 Mexico 127,575,529 Nigeria 200,962,417 Pakistan 204,596,442 Poland 38,028,278 Russia 143,895,551 S. Korea 51,339,238 S. Africa 58,065,097 Tunisia 11,718,694 UK 66,959,016 US 329,093,110

Growth rate (%)

GDP/capita in USD

Median age

Urban pop (%)

1.28 0.56 0.72 0.88 0.35 0.18 1.08 0.90 1.49 −0.13 −0.26 1.09 2.60 1.88 −0.20 −0.05 0.34 1.16 0.95 0.58 0.71

50,400 46,600 15,600 48,400 16,700 50,800 7200 73,200 36,400 38,200 42,900 19,900 5900 5400 29,600 27,900 39,500 13,600 11,900 44,300 59,800

38 42 33 41 39 47 28 39 30 48 48 29 18 23 42 40 43 27 32 41 38

90 96 86 83 60 76 34 65 92 72 94 80 52 40 61 73 82 63 69 81 84

Source: World Factbook (2020)

proposed policy changes made by the government. Likewise, the influence of the medical industry and medical and nursing associations varies widely, as does the power of insurance providers in shaping health policy. In addition to the values and institutions of a country, health policy is shaped by the composition of its population and by demographic patterns. Heterogeneous, multicultural populations require more complex health systems than more homogeneous ones. Likewise, older populations have needs different from younger ones. Populations can also be stratified by class, economic status or other social groupings. The way in which medical resources are distributed also reflects the current state of medical technology and the public expectations and demands that accompany it. Population growth rates are also crucial because they point to future health needs and relate to the dynamic composition of the population. A high growth rate requires planning for expanded services, and depending on where the growth is coming from (e.g. births, immigration), a change

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in types of services is needed. In contrast, a low or negative growth rate might indicate difficulties in funding services even at the existing level. Not surprisingly, health policy is influenced significantly by a country’s financial resources. Studies across developed and developing countries find that the per capita income of a country is the single most important factor when explaining health expenditure variation. Some countries often have difficulties meeting even minimal health needs, much less the types and range of services needed by patients with ALS/MND. By including a wide range of countries on this measure, we should obtain a much more complete picture of existing ALS/MND policy as well as the policy challenges it raises.

Summary of Individual Chapter Objectives Chapter authors were asked to discuss key aspects of public policy in their respective countries as it relates to ALS/MND funding, patient care and family caregiver support. One emphasis was on governmental agencies and actions, special reports pertaining to ALS/MND patient care and research support, as well as activities of private foundations and advocacy groups. Other foci included the location of care provided; access to assistive technologies; the availability of ALS/MND multidisciplinary clinics; use of advance directives; and the legal status of palliative sedation, withholding and withdrawing life-extending care, PAS and euthanasia. Authors were also asked what social and cultural factors unique to their country might help explain ALS/MND policy and what changes and improvements in policy could lead to enhanced patient care and research support for ALS/MND. To address these concerns and provide a starting point for coverage and facilitate comparative data, chapter contributors were asked to address, where appropriate for their country, the below questions and issues. To avoid repetition, authors were asked not to include the background information on ALS/MND which has been provided in this chapter. 1. Incidence and prevalence and deaths of ALS/MND in their country. 2. What, if any, governmental action, reports, committees on ALS/ MND exist? 3. Major governmental agencies involved in care—national, state, local. 4. The most active private ALS/MND organizations, associations, advocacy groups.

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5. Policy associated with ALS/MND research and the relative contributions from the public versus private sectors. 6. How much public funding for research and care? Is it satisfactory? 7. Public/media/commercial perceptions of ALS/MND. 8. What proportion of ALS/MND patients live at home vs institutional care? 9. Composition of caregivers—informal, formal (paid). Any trends? 10. Governmental aid for family caregivers—financial or respite care? 11. Access to assistive technologies such as electronic communication devices? 12. Status of multidisciplinary team care and clinics. 13. “Right to try” legislation advocating for ALS/MND patients to be treated with drugs that have not yet been approved. 14. Genetic testing for ALS/MND. Who pays? What protections for confidentiality are provided for patients and blood relatives being tested? 15. What proportion dies at home, in nursing facility, hospital or hospice? 16. Access to palliative and hospice care, with estimate of percent of ALS/ MND patients eventually enrolled in hospice care? 17. Legal status of advance directives and withholding or withdrawing mechanical ventilation and other life-extending interventions and mechanical support. 18. Legal status of palliative sedation, euthanasia and physician-­ assisted suicide. 19. What factors unique to the country (cultural, social, religious, economic, etc.) are critical for understanding decision-making in that country? 20. What, if any, changes in policy are needed to improve care of ALS/ MND patients and support for family caregivers and to advance research support for the cure or development of disease-modifying treatments? We thank the numerous authors who gave generously their time and collaborative efforts while providing insights and expertise necessary for the publication of this book. We hope those reading this volume will find it a useful guide to international perspectives on public policy for ALS/ MND and will help facilitate the development of future collaboration and exchange of ideas across even more countries. The concluding chapter will discuss policy options and summarize how best to ensure workable and humane ALS policy for the coming decades. An underlying theme is that such a policy requires a cross-national, multidisciplinary effort.

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Brooks, B., R. Miller, M. Swash, and T. Munsat (2000). Diseases WFoNRGoMN. El Escorialrevisited: Revised criteria for the diagnosis of amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis and other Motor Neuron Disorders 1: 293–99. Brown, R.H. and A. Al-Chalabi (2017). Amyotrophic lateral sclerosis. A review. New England Journal of Medicine 377: 162–72. Carver, A.C. (1996). End-of-life care: A survey of US neurologists’ attitudes, behavior and knowledge. Neurology 53: 284–93. Cedarbaum, J.M., N. Stambler, E. Malta et al. (1999). The ALSFRS-R: A revised ALS functional rating scale that incorporates assessments of respiratory function. Journal of Neurological Sciences 169: 13–21. Chen, A., L. Weimer, T. Brannagan et al. (2010). Experience with the Awaji Island modifications to the ALS diagnostic criteria. Muscle and Nerve 42: 831–32. Cherny, N.I., L. Radbruch et al. (2009). European Association for Palliative Care (EAPC) recommended framework for the use of sedation in palliative care. Palliative Medicine 23: 581–93. Chio, A., G. Logroscino, B.J. Traynor et al. (2013). Global epidemiology of amyotrophic lateral sclerosis: A systematic review of the published literature. Neuroepidemiology 41: 118–30. Chio, A., L. Mazzini, S. D’Alfonso et al. (2018). The multistep hypothesis revisited—The role of genetic mutations. Neurology 91: e635–42. Corcia, P., P. Couratier, H. Blaco et al. (2017). Genetics of amyotrophic lateral sclerosis. Revue Neurologique 173: 254–62. Costa, J., M. Swash, and M. de Carvalho (2012). Awaji criteria for the diagnosis of amyotrophic lateral sclerosis: A systematic review. Archives of Neurology 69 (11): 1410–16. Couratier, P., P. Corcia, G. Lautrette, M. Nicol, and B. Marin (2017). ALS and frontotemporal dementia belong to a common disease spectrum. Review of Neurology (Paris) 173: 273–79. Goldstein, L.H. (2014). Control of symptoms: Cognitive dysfunction. In D. Oliver, G.D. Borasio, and W. Johnston, eds., Palliative Care in Amyotrophic Lateral Sclerosis: From Diagnosis to Bereavement, 3rd edition. Oxford: Oxford University Press, pp. 107–25. Gursahani, R. (2016). Palliative care and the Indian neurologist. Annals of Indian Academy of Neurology 19 (Suppl 1): S40–44. Horner, R.D., K.G.  Kamins, J.R.  Feussner et  al. (2003). Occurrence of amyotrophic lateral sclerosis among Gulf War Veterans. Neurology 61: 742–49. Johnston, M., L. Earll, E. Mitchell et al. (1996). Communicationg the diagnosis of motor neurone disease. Palliative Medicine 10: 23–34. Lomen-Hoerth, C.J., S. Murphy, S. Langmore et al. (2003). Are amyotrophic lateral sclerosis patients cognitively normal? Neurology 60: 1094–97. Ly, C.V. and T.M.  Miller (2018). Emerging antisense oligonucleotide and viral therapies for amyotrophic lateral sclerosis. Current Opinions Neurology 31 (5): 648–54.

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Maessen, M., J.H. Veldink, L.H. van den Berg et al. (2010). Requests for euthanasia: Origin of suffering in ALS, heart failure and cancer patients. Journal of Neurology 2010: 1192–98. Magyari, M. and P.S. Sorensen (2019). The changing course of multiple sclerosis: Rising incidence, change in geographic distribution, disease course, and prognosis. Current Opinions in Neurology 32 (3): 320–36. Malek, A., A. Barchowsky, R. Bowser et al. (2013). Exposure to hazardous air pollutants and the risk of amyotrophic lateral sclerosis. Environmental Pollution 197: 181–86. McKee, A.C., B.E. Gavett, R.A. Stern et al. (2010). Correspondence regarding TDP-43 proteinopathy and motor neuron disease in chronic traumatic encephalopathy. Journal of Neuropathology and Experimental Neurology 42: 851–52. McKhann, G.M., M.S. Albert, M. Grossman et al. (2001). Clinical and pathological diagnosis of frontotemporal dementia report of the work group on frontotemporal dementia and pick’s disease. Archives of Neurology 58: 1803–9. Miller, R.G., J.A. Rosenberg, D.F. Gelinas, H. Mitsumoto et al. (1999). The care of the patient with amyotrophic lateral sclerosis (an evidence-based review): Report of the quality standards subcommittee of the American Academy of Neurology: ALS practice parameters taskforce. Neurology 52: 1311–23. Miller, R.G., C.E.  Jackson, E.J.  Karsarkis, J.D.  England et  al. (2009). Practice parameter update: The care of the patient with amyotrophic lateral sclerosis: Multidisciplinary care, symptom management, and cognitive/behavioural impairment (an evidence-based review). Neurology 73: 1227–33. Miller, T., M. Cudkowicz, P.J. Shaw et al. (2020). Phase 1-2 trial of antisense oligonucleotide Tofersen for SOD1 ALS.  New England Journal of Medicine 383: 109–19. Mueller, C., J.D. Berry, D.M. McKenna-Yasek et al. (2020). SOD1 suppression with adeno-associated virus and microRNA in familial ALS.  New England Journal of Medicine 383: 151–58. National Hospice and Palliative Care Organization (2010). Position statement and commentary on imminently dying terminally ill patients. Journal of Pain and Symptom Management 2010: 914–23. National Institute for Health and Care Excellence (2016). Motor neurone disease: Assessment and management. NICE Guideline NG 42. www.nice.org.uk/ guidance/NG42 Neudert, C., D. Oliver, M. Wasner and G.D. Borasio (2001). The course of the terminal phase in patients with amyotrophic lateral sclerosis. Journal of Neurology 248: 612–16. Oliver, D.J. and M.R.  Turner (2010). Some difficult decisions in ALS/ MND. Amyotrophic Lateral Sclerosis 11: 339–43 Phukan, J. (2012). The syndrome of cognitive impairment in amyotrophic lateral sclerosis: A population-based study. Journal of Neuropathology and Experimental Neurology 83: 102–08.

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CHAPTER 2

Public Policy in MND Care: The Australian Perspective Samar Aoun, Carol Birks, Anne Hogden, and Susan Mathers

Abstract  Financial support, access to respite care, ‘in-home support’ and assistive technologies and access to specialist palliative care for MND patients vary between and within the Australian states and the age groups of patients. While care takes place mainly at home, proportions dying at S. Aoun (*) Perron Institute for Neurological and Translational Science, Perth, Australia e-mail: [email protected] La Trobe University, Melbourne, Australia e-mail: [email protected] C. Birks MND Australia, Canberra, Australia e-mail: [email protected] A. Hogden University of Tasmania, Sydney, Australia e-mail: [email protected] S. Mathers Calvary Health Care Bethlehem and Monash University, Melbourne, Australia e-mail: [email protected] © The Author(s) 2021 R. H. Blank et al. (eds.), Public Policy in ALS/MND Care, https://doi.org/10.1007/978-981-15-5840-5_2

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home vary between 25 and 34 percent. MND multidisciplinary clinics operate in the capital city of each mainland state. Most states have statutory Advance Health Directives, but voluntary assisted dying is only available in the states of Victoria and Western Australia to date. To improve care and advance research, improvements are needed at three levels: the government, the workforce and the community. Public services need to be delivered in a more timely, efficient, integrated and equitable manner. In order to inform future planning and policies for solutions to the growing demand for family/informal care and the associated challenges encountered by family carers, it is essential to integrate family carers’ needs into service planning. Keywords  MND associations • Research funding • Multidisciplinary teams • Assistive technology • Genetic testing • Palliative care • Voluntary assisted dying • Integrated care • Funding models

Incidence, Prevalence and Deaths of MND in Australia An accurate figure for the incidence of MND in Australia is difficult to ascertain as there are no official records of every person diagnosed nor mandatory reporting. In Australia, MND associations maintain a record of people with a confirmed diagnosis of MND who join as members. From July 2018 to June 2019, 756 people recently diagnosed with MND had joined a state MND association (Motor Neurone Disease Australia 2019). However, diagnosis may have taken some time or people may not have joined immediately following diagnosis. The Australian MND Registry also registers people with MND who are referred to a specialist MND clinic, however, this registry does not capture people diagnosed with MND who are not referred to these clinics or who cannot access them due to distance. A Deloitte Access Economics Report commissioned by MND Australia in 2015 estimated the mortality rate to be 3.14/100,000 across the entire population (Deloitte Access Economics 2015). It could be assumed that mortality rate and incidence rate are similar, which would indicate that based on the current population of Australia of 25,088,636, the incidence rate is approximately 788 persons per year.

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The Deloitte Access Economics Report found that Australia has a relatively high level of prevalence in comparison to other countries, and it was estimated that there were 2094 Australians living with MND in 2015. Of that 60 percent were males and 40 percent were females. The highest prevalence rate was reported in males aged between 75 and 84. Based on the analysis undertaken in this report, the overall prevalence of MND in Australia is estimated to be 8.7/100,000 Australians, or 1  in 11,434 Australians. Each year MND Australia makes a special request to the Australian Institute of Health and Welfare (AIHW) for data from the National Mortality Database on deaths with MND as underlying cause and deaths with MND as an associated cause. Adding both associated causes and underlying causes of death gives the total known deaths associated with MND in Australia. This data indicates that there were 755 known deaths of people with MND in 2018 due to any cause, of which 692 deaths were specifically due to MND (MND was listed as an underlying cause) (Motor Neurone Disease Australia 2018a).

Governmental Agencies Involved in Care The complex and progressing nature of MND requires an interdisciplinary approach encompassing health, disability, community, aged, respite and carer support services. The Australian healthcare system provides people with access to general practitioners (GPs), neurology, respiratory, gastroenterology, neuropsychology, rehabilitation, nursing, palliative care and allied health services to address their medical needs and to monitor progression. Universal access to healthcare is available through the national publicly funded Medicare system, supported (for some people) by private health insurance, with either local, state or federal governments being responsible for delivery of services. Access to allied health can be complex with some allied health providers funded through the health system and others through the recently introduced National Disability Insurance Scheme (NDIS). The NDIS provides fully funded reasonable and necessary disability supports to Australians with a permanent disability who are aged 64 or younger when they enter the scheme (Carer Gateway 2019). The last few years have seen a national roll out of the NDIS with a full roll out completed on 1 July 2019. This scheme is a transformational change in the way disability supports are

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provided and funded in Australia. The scheme is funded by the Australian government and to date all sides of politics have pledged to fully fund the scheme. For people aged 65 years or older when diagnosed with MND, their disability support must be accessed through the aged care system. Unlike the NDIS where anyone with a permanent disability, including people with MND, is entitled to access the scheme, older people with MND must be assessed as eligible to access an aged care community home care package. These packages are funded by the Australian government with a cap on the number of packages available, a means-tested co-payment and a limit on funds available to support assessed needs. Access to assistive technology may be through a person’s MND association, their NDIS plan or a state government-funded equipment service. Similarly, respite and carer support services may be accessed through or funded by MND associations, the NDIS or Australian government carer respite services.

Active MND Associations and Advocacy Groups MND associations were established in each of the Australian states and the Australian Capital Territory (ACT) over 37 years ago to support people living with MND; their family, friends and carers; and the health and community providers involved in their care (Motor Neurone Disease Australia 2018b). The ACT association merged with MND New South Wales (NSW), and today the six state MND associations provide direct services and support through the National MND Support Service Model to people living with MND and their family and friends across Australia (Motor Neurone Disease Australia 2018c). MND Australia was established in 1991 by the state MND associations to provide a national voice for MND. MND Australia is focused on improving the lives of all Australians impacted by MND by influencing policy through advocacy, providing and developing trusted information in various formats, raising awareness and understanding of MND nationally and promoting and funding the best research. MND Australia is committed to building partnerships and strategic alliances to more effectively liaise with government to ensure that policies support the interests of people living with MND.  To advocate effectively, MND Australia works to co-advocate with related organizations in the research, medical and care sectors such as the Neurological Alliance Australia, Palliative Care

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Australia, Carers Australia, Research Australia, Stem Cells Australia and Rare Voices Australia. MND Australia has been an active member of the International Alliance of ALS/MND associations for over 26 years. More recently, MND Australia has focused specifically on supporting collaborations and partnerships in the Asia Pacific region. There are several other MND organizations in Australia. The MND and Me Foundation was established in 2010  in Queensland to provide additional support to Queenslanders impacted by MND and to fund vital research (MND and Me 2019). Fight MND (formerly known as Cure MND) was established in 2014 to raise awareness and funds for research, mainly clinical trials, and assistive technology (Fight MND 2019).

Funding for Research and Care In Australia, funding for MND research is provided by a combination of government, private, non-government/not-for-profit and philanthropic sectors. Care is mostly funded through state and federal government agencies related to health, disability and aged care. The MND Research Australia (former name MNDRIA) is the research arm of MND Australia and has been funding MND research with the greatest chance of moving us closer to a world free of MND for over 30 years. A recent report 25 Million 25 Milestones: Changing the Future of MND highlights the impact of MND Research Australia funding in Australia over this time (Motor Neurone Disease Australia 2017a). The ALS/MND community and the state-based MND associations have always been effective fundraisers, channeling funds to care, equipment, as well as research through MND Research Australia. Since its inception in 2014, Fight MND has raised substantial funds (over $28.5 million to mid-2019) for research, thereby changing the research landscape in Australia through accelerating precision medicine and access to clinical trials. As well as funding competitive research grants through the National Health and Medical Research Council (NHMRC), the medical research future fund (MRFF) and other commonwealth agencies, the federal government in recent years has contributed funding to Fight MND to fund research focused on clinical trial pathways in Australia. Although several specialist MND clinics have developed across Australia, this has largely been driven by local partnerships and small groups of motivated individuals. These groups are now working together at a national level to increase access to research and clinical trials for people with

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MND. The sustainability of these alliances, however, still relies on piecemeal funding from competitive grants and philanthropy, despite education and research being part of the remit of state-funded tertiary and quaternary health services.

Proportion of Patients Who Live at Home vs. Institutional Care The aim of care in Australia is to support people to live and die in the setting of their choice. Most people with MND prefer to remain at home and in their community to receive care and most people achieve this goal. Others may remain at home with support from family, friends and government-­funded health and community home-based support and then choose to enter a hospice or hospital for end-of-life care. For Australians who do not have enough family and community support to stay at home, an admission to a residential aged care facility is then required. With the introduction of the NDIS, it is more likely that older people are in this situation. There are no accurate figures for people with MND living in residential aged care. However, according to deaths in Table 2.1, the proportion could be between 16% and 28% depending on the Australian state.

Composition and Support for Caregivers The demographic information on informal caregivers is gleaned from a national survey undertaken in Australia to explore the experiences with receiving the diagnosis of MND (Aoun et al. 2017a). The mean age of responding family caregivers (n = 190) was 62.1 years (SD = 12.4, range 25–88): 67.2 percent were females, 93.8 percent were married, 82.8 percent were the spouses or partners of the person with MND, 11.7 percent Table 2.1  Proportions in each place of death (percent) 2017–18 Place of death Home Hospital Hospice/palliative care unit Nursing home Unknown

Victoria

WA

NSW

25 23 22 28 2

34 28 17 16 4

25 24 21 18 11

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were their adult children and 52.9 percent of family caregivers were retirees. Although there is no official information on the composition of paid caregivers in the MND setting, they are employed under two governmentfunded schemes, the NDIS for the group under 65 years and the My Aged Care packages for the group 65 years and over. Australia has a national strategy for supporting family caregivers (Carer Recognition Act 2010) and National Palliative Care Strategy (2018) (Carer Recognition Act 2010 (Austl.); Australian Government 2018). Government financial support exists for people with significant disability including those with terminal illness that indirectly benefits carers; however, direct support is generally income and asset tested. A carer payment provides income support for inability to work because of the demands of caregiving. There is also a carer allowance which is a smaller income supplement for daily caregiving to those aged or with severe disability. Support for out-of-pocket costs such as travel and accommodation is available for patients, but not their caregivers, and there is a subsidy for patients living more than 100 km from a healthcare provider. There are concessions for carers traveling with a disabled person in the form of carer’s card or companion card for those with significant and permanent disability (WA Companion Card 2016). The Taxi User’s Subsidy Scheme (TUSS) is another resource that can be accessed at a reduced rate (Department of Transport 2019). Respite care provision is poor and the NDIS can provide planned respite. There is a work and care charter which promotes flexible working hours and flexible leave for caregivers, but it is voluntary with no obligations from employers. Carers of those with a disability may be eligible for reduced tax on income and for pension supplement for those receiving an existing carer’s payment. However, forms to access carers’ allowance and payments are generally aimed at long-term disability, not shorter, quicker deterioration as is the case with most MND cases. Furthermore, there are two energy-related schemes to help people in certain circumstances meet their energy needs: The Energy Concession Extension Scheme and the Thermoregulatory Dysfunction Energy Subsidy Scheme (www.finance. wa.gov.au).

Access to Assistive Technologies According to a Deloitte Access Economics Report (Deloitte Access Economics 2015) commissioned by MND Australia in 2015, aids and equipment comprise one of the highest per-person costs. The often-rapid

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rate of progression requires fast-track access to a wide range of equipment since items need to be available as soon as a need arises and may only be required for a short period of time. The report states that aids and equipment cost $31,598 per person in 2015 and confirmed the MND association equipment loan service as a cost-effective model in providing equipment to maintain independence and communication. For people living with MND, the full range of assistive technology may include aids and equipment to support comfort, independence and daily living, communication technology and non-invasive ventilation to support breathing, and quality and length of life. Non-invasive ventilation improves survival by 13 months on average (Berlowitz et  al. 2016). Under the NDIS, people living with MND aged 64 and under are entitled to “reasonable and necessary” assistive technology to meet their needs. Where available and appropriate, a person’s NDIS plan includes funding to cover hire or rental costs to enable fast-track access to individual items or a bundle of assistive technology provided by the MND association. In addition, it includes funding for reasonable and necessary home modifications and specialized individualized assistive technology. People aged 65 or older when diagnosed with MND access assistive technology through state government assistive technology loan services, which often entail long waiting times. MND associations in Australia have built assistive technology loan pools or equipment libraries through funding received from donors, state government funding and philanthropic grants. This vital service helps people living with MND to access assistive technology in a timely manner. The range of technology available from MND associations does vary, and therefore timely access to government-­funded assistive technology schemes continues to be a focus for advocacy. People living with MND must undergo an assessment by an appropriate allied health professional, and a referral made before assistive technology is supplied by an MND association or a government-funded scheme. This professional will then train the person with MND and their carer in the correct use of the technology. Specialized respiratory support is usually provided through the person’s MND clinic or health service, but access varies by state. From 1 October 2019, the NDIS has started to fund health-related supports if they are a regular part of the participant’s life and a result of their disability. This includes respiratory and nutritional support.

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Status of Multidisciplinary Team Care and Clinics Specialist neurology-led MND multidisciplinary clinics operate in Sydney, Melbourne, Brisbane, Adelaide, Canberra and Perth. Most of these clinics work out of public hospitals. In some regional and rural communities, local health practitioners have established MND-specific multidisciplinary models of care to support a coordinated approach to people living with MND in their community. Some MND multidisciplinary clinics offer e-Health (or telehealth) services to support patients and families in nonmetropolitan areas, linking with local service providers where possible (Henderson et al. 2014; James et al. 2018).

“Right to Try” Legislation for ALS/MND Patients There is no legislation regarding right to try in Australia; however, after discussion with their neurologist, individuals may be able to apply to access products that have not yet been approved in Australia through a Special Access Scheme (SAS). There are three SAS pathways that a health practitioner may use to access an unapproved therapeutic good for an individual patient on a case-by-case basis. Category A is a notification pathway (for a patient defined as seriously ill) that may be accessed by a prescribing medical practitioner; Category B is an application pathway that can be accessed by health practitioners (usually medical or dental practitioners) if patients do not fit the Category A definition; Category C is a notification pathway that allows certain types of health practitioners to supply therapeutic goods that are deemed to have an established history of use (Motor Neurone Disease Australia 2017b).

Genetic Testing of Patients with MND Costs for genetic testing vary considerably in Australia. Cost depends on the type of testing being conducted (diagnostic, predictive or confirmatory), the genes being tested and the type of genetics service that is accessed. For example, the cost of testing a single gene, most commonly SOD1 or C9orf72, varies according to which gene is being tested. Similarly, the cost of testing a panel of genes is considerably higher than for a single gene. Moreover, the cost of predictive genetic testing in a family member with an identified gene mutation is less expensive than for diagnostic testing for that family (Crook et  al. 2017). Some public hospital genetic testing services

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provide subsidized or free testing for MND-related genes, particularly for patients or relatives who are from a family with a history of MND. However, private genetic testing services will vary in what they charge. These costs are not covered by Medicare, the national government health insurance scheme. Genetic testing for research purposes entails no cost to the patients or family members who agree to participate in the research. The decision to have genetic testing is voluntary, and the results are confidential, as with any medical intervention. Although an appointment with a genetic counselor is not required when the results are given, genetic counseling is recommended with pre- and post-testing (Hogden and Crook 2017). When family members are treated at the same time, the results are typically given individually to preserve confidentiality. Even so, family members may choose to have each other present for support. Testing results cannot be shared without the express consent of the person being tested, except as required by law. This includes sharing with health professionals and other family members. If testing is conducted for research, confidentiality is protected through research processes approved by a human ethics research committee. Further information about genetic testing is available for people with MND and their families from MND Australia (Motor Neurone Disease Australia 2018d).

Place of Death: At Home, in Nursing Facility, Hospital or Hospice Recent mortality data (2017–18) obtained from three MND associations (personal communication), two large ones on the east coast (Victoria and New South Wales [NSW]) and one small on the west coast (Western Australia [WA]), suggest a total of 892 MND deaths in the past two years in the three Australian states. Looking at the proportions in Table  2.1, more deaths occurred at home and in hospital in Western Australia compared to Victoria and NSW where more deaths occurred in a nursing home or in a hospice. This reflects differences in access to and/or availability of inpatient and community services in each state.

Access to Palliative and Hospice Care In a recent national survey of bereaved people, more people with cancer (64%) had received palliative care services in comparison to other non-­ malignant illnesses (4–10%), with non-malignant diseases still

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under-­represented in palliative care in Australia (Aoun et al. 2017c). There is a very short period of a median of one month that patients were under a specialist palliative care service. There is increasing evidence that palliative care integrated in a multidisciplinary approach to care leads to improved symptoms and quality of life of people with MND and their families (Oliver et al. 2016). It is recommended that a palliative approach be integrated into the care plan from the time of diagnosis to optimize quality of life by relieving symptoms; providing emotional, psychological and spiritual support pre-­bereavement; minimizing barriers to a good death and supporting the family post-­ bereavement. These outcomes can only be achieved if palliative care knowledge and expertise is extended beyond the domain of specialist palliative care services to include the full scope of health and community-­ based services providing care, mostly at home, in order to meet the extensive range of needs of people with MND and their family carers from diagnosis to bereavement (Aoun 2018). In Western Australia, MND patients are usually accepted into a specialist palliative care service only in the last three months of life, if they need ongoing treatment for significant unrelieved symptoms such as breathlessness, secretion management, pain and non-invasive ventilation. They are discharged if their condition improves or remains stable. People with MND in nursing homes will usually end up at hospice to receive palliative care, while those who remain at home will receive some palliative care toward the end, but only after this is arranged by their referring GP, neurologist or respiratory physician. Therefore, in line with improving the palliative approach to care and because palliative care has become synonymous with service provision in the last months or weeks of life, the MND association in Western Australia has embarked on state-wide educational program for health and community-based services at the start of 2019, which has received very positive feedback. Palliative care is supported in Victoria by MND Palliative Care Shared Care Workers, one funded in each region. They are the “go to person” in palliative care regarding MND and they work closely with MND association advisors. Palliative care is supported by additional funding for inpatient and community-based services to recognize the extended services that may be required by people with MND, including top-up funding (Victorian Government 2008).

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Legal Status of Advance Directives and Withholding or Withdrawing Life-Extending Interventions and Mechanical Support The legal status of Advance Health Directives (AHD) is complicated by differences between state and territory laws. Advance Care Planning (ACP) is supported in Australia by both statute law and common law (Advance Care Planning Australia 2018). However, the laws and legislative frameworks vary from state to state. All states and territories have statutory Advance Care Directives (ACDs), excepting New South Wales and Tasmania. In these states, ACDs are recognized as valid in common law. All ACDs in Australia can include refusal of specific, or all, treatments (except palliative care) and withdrawal of life-extending measures. Most states and territories recognize ACDs of other states and territories, except the Australian Capital Territory and Tasmania. This has implications for people with MND intending to visit, receive services or relocate interstate. However, according to a recent national survey of bereaved people, the uptake of such AHD and ACP documents is still low in Australia at about 10 percent, although those who received palliative care were two to three times more likely to have an ACP or AHD in place (Aoun et al. 2017c).

Legal Status of Euthanasia and Physician-Assisted Suicide Euthanasia is illegal in Australia, but Victoria and Western Australia are the only two states to recently enact similar voluntary assisted dying laws. From June 2019, Victorians who are suffering from an incurable, advanced and progressive disease, illness or medical condition, and who are experiencing intolerable suffering, are eligible (Health Victoria 2019). The condition must be assessed by two medical practitioners as being expected to cause death within six months. Exceptions are for people suffering from a neurodegenerative condition, such as MND or multiple sclerosis, where the condition must be expected to cause death within 12 months. Voluntary assisted dying is only available to people over the age of 18 who have lived in Victoria for at least 12 months and who have decision-­ making capacity. To be eligible, people must be experiencing suffering that cannot be relieved in a manner the person considers tolerable. In the

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Victorian model, the responsibility of assisted dying lies with the patient. However if the patient is physically incapable of self-administering, the doctor needs to apply for a practitioner administration permit. The voluntary assisted dying laws for Western Australia were passed on 10 December 2019 with an 18-month implementation period. Voluntary assisted dying in WA may be through self-administration or practitioner administration of the dying substance. The death certificate must not include any reference to voluntary assisted dying.

Critical Factors for Understanding Policy Making in Australia Healthcare Structure and Funding Arrangements The Australian healthcare system has a complex structure dominated by the constitutional boundary between federal and state responsibilities. The major responsibilities of the Australian government include health service funding, regulation of health products, services and workforce, primary and aged care and veteran’s affairs. The federal government has responsibility for the universal public health insurance scheme, Medicare (including subsidizing medical services and providing funding for primary health networks). The Australian government partially funds eight state and territory health systems. These systems are primarily responsible for the delivery and management of public health services, including public hospitals, community health and public dental care, and the regulation of healthcare providers and private health facilities. Public hospitals, for example, are licensed, regulated and funded by the Australian, state and territory governments, but managed by state and territory governments. Local governments fund and deliver some health services such as environmental health programs. The Australian healthcare system is a combination of both public and private health organizations and individual providers. Australia provides universal healthcare to the population regardless of geographical location or financial capacity. This includes access to emergency medical care via ambulance/paramedicine services, emergency departments and intensive care units. However, these systems are now underpinned by co-payment arrangements, whereby patients in many instances contribute

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directly—through private health insurance or payments for medicines, tests or specialists—and indirectly—via taxation arrangements—to fund the care they receive (Australian Institute of Health and Welfare 2016). Geography Australia’s vast geography combined with a relatively small population that is concentrated around coastal areas has a significant impact on how easily Australians can access the health services they need (Hogden et al. 2017). This is particularly so for people with MND in accessing specialized MND and palliative care services. Specialized MND multidisciplinary clinics exist in only six metropolitan areas, meaning that people living in regional or rural areas may have to travel long distances (hours or even days) to receive services. This puts regional and rural patients at a disadvantage if fatigue and mobility problems restrict them. While telehealth offers a solution for many therapeutic interventions, palliative care, particularly at the end-of-life, requires hands-on service (Henderson et al. 2014; James et al. 2018). The training of local health providers in an integrated palliative approach may go a long way toward reducing the tyranny of distance (Hogden et al. 2018). Cultural Diversity Australia is culturally diverse: one in four Australians was born overseas, identifying with more than 270 ancestries; and 20 percent of Australians speak a language other than English at home (Australian Human Rights Commission 2015). Over 200 languages are spoken in this multicultural society. MND occurs in all populations; therefore, services for people with MND and their families also need to provide for a range of languages, health literacy abilities and cultural beliefs. Health services increasingly have become more tailored to the characteristics of the local community. For example, specialized services are provided for aboriginal health by members of the indigenous community. Service providers need an understanding of the end-of-life considerations of their local communities, including chaplaincy, attitudes to information-sharing, death customs (including preparation of the body and timing of burial after death) and Australian laws and procedures (which differ from state to state).

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Policy Changes Needed to Improve MND Care and Advance Research Support For over two decades, the policies of both federal and state levels of government in Australia have promoted an integrated, patient-centered approach to service delivery. Despite this, care is still seen as fragmented by many consumers and care providers. According to the Productivity Commission (2017): progress towards an Australia-wide integrated system of care across primary, hospital and other sectors has been poor, hampered by weak information flows and coordination, inadequate attention to the experiences of patients and flawed incentives and inadequate governance arrangements (in large part created by the Commonwealth/State divide in funding arrangements).

What are the barriers, then, to a functioning system, capable of meeting the needs and preferences of people living with MND on a day-to-day basis? Barriers exist in at least three different but interacting domains: government, workforce and community. Government and the Bureaucracy The public contributes financially and, through the ballot box, philosophically to how the health and welfare systems run. It is ironic, perhaps tellingly so, that a government trying to deliver the wide range of necessary public services to citizens, in an efficient and equitable manner, should itself have a dichotomous structure, separating federal and state jurisdictions, as well as authority over health and disability funding and reporting. An “all of government” approach is needed to meet an expectation that reasonable health, disability and social needs will be met in future. Such an overarching authority could use algorithms to fast-track people diagnosed with rapidly changing diseases like MND through the bureaucracies when employment, financial, family and domestic well-being are threatened by a progressive, life-limiting illness. With the current roll-out of the National Disability Insurance Scheme (NDIS), there is a growing acknowledgment that living well with a chronic disease is not all about healthcare and that planning disability supports must anticipate the changing needs related to disease trajectories. It remains inequitable that people with MND under

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the age of 65 years receive vastly superior levels of disability support through the NDIS compared to those diagnosed after 65 years through the aged care system. Government and the Workforce  eam-Based, Multidisciplinary Care T Multidisciplinary, team-based care is beneficial to people living with MND, improving symptom management, quality of life and survival (Hogden et al. 2017; Oliver et al. 2016), yet there is no government-driven integration of care delivery across sectors and no targeted funding for this model of care. “Medicare does not provide care which is coordinated and integrated around the needs of patients; and it does not help the people providing the care to do this” (Health 2040. Victorian Government discussion paper).  unding Models for Innovation F Funding models need to support innovation in the workforce to allow the system to operate in a more unified way. Local solutions and partnerships between motivated regional players have been shown to produce more successful collaborations and better flow of information (Goodwin et al. 2013). The current system also fails to identify a named care coordinator, who the patient can choose to manage all their services and improve communication across their care team. Most “coordinators” manage aspects of a patient’s services (NDIS or aged care funding, healthcare, palliative care), but may lack the big picture view and the ability to advocate with certain providers. Workforce Capability/Education Studies have also shown that the workforce is often not trained or supported to function as a team and commonly fails to communicate outside of their own workplace (Banfield et al. 2013). The Neurological Alliance Australia, in a joint statement with Palliative Care Australia, called for improved access to palliative care services for people living with neurological conditions, but it also identified a need for education for palliative care staff to improve their knowledge, understanding and confidence in providing care to people with these conditions.

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Workforce Deployment Although the government has placed a greater emphasis on advance care planning in recent years, achieving the person’s goals for management is often confounded when symptoms or contingencies occur out of hours when many GPs rely on locum services. It is therefore difficult for them to provide medical leadership in the care of patients who have chosen to die at home. Also, many palliative care services do not provide home visits after hours, relying on phone advice and the resources of families to administer drugs and monitor effect. Therefore, emergency departments become the default provider for managing symptoms or social breakdown—swelling the number of people who, although they want to die at home, end up dying in hospital. In Australia, there is poor integration of mental health services with neurological care for people with organic neurological illnesses. Addressing anxiety, mood and behavioral disturbance, which are often co-morbid with neurodegenerative conditions, should be indivisible from the management of the physical symptoms of the disease. Both require skilled care from knowledgeable staff working in partnership. Accommodating people when they require inpatient, respite or residential care also needs policy to promote a person- and family-centered approach to achieve age-­ appropriate settings, the right staff skill mix and least restrictive outcomes. As chronic diseases are now the leading cause of death around the world, government policy should foster comprehensive care models that are sustainable around the clock and across distance from specialist centers. Increasingly, we see these types of models used in triage and acute intervention in stroke, trauma and the newborn, often supported by telemedicine. Because of their comprehensive knowledge base and multidisciplinary make-up, specialist MND services, if appropriately resourced and indemnified, could support other practitioners in the wider community, including assessment or advice in urgent situations. Government and the Community Health Literacy According to the Australian Bureau of Statistics, almost 60 percent of adults in Australia have poor health literacy. This is associated with increased rates of hospitalization, emergency care and poor outcomes, as well as increased healthcare costs. Publicly funded campaigns to educate the general population about the risks of smoking or to raise awareness of

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HIV/AIDS have been very successful in changing behavior. Educating people about their own bodies, disease prevention, supported decision-­ making and how their taxpayer-funded services work should be even easier with so many media platforms now available. Policy could also give focus to addressing the special needs of groups where social determinants of low health literacy are already known (poor health status, high use of health services, low socio-economic status, less educated and older age). S hared Information Systems The lack of shared information systems also impairs communication and fosters fragmented care decisions. An opt-out, national e-health record (My Health Record) is being launched and could be beneficial if patients and providers are trained in its use. Ideally, the patient should be able to consent to some or all the content being shared with their care team. My Health Record has also been suggested as a conduit for accessible health information and prompts. Surveys and data-linkage could also assess individual health literacy, patient experiences and other health metrics. With the financial support of an NHMRC Partnership grant, a consortium of MND clinicians, researchers and MND associations in Australia are working toward effective data-linkage of current registries and databases. Patients, carers and providers will also be able to input their own data and access information and resources through a consumer-controlled App or Website. Although assistive technologies help people with MND overcome verbal or written communication difficulties, hospital systems and bureaucracies still usually communicate by phone or letter. Email and texting are viable alternatives for people with these disabilities and should be encouraged, especially if secure platforms are provided. S ustaining the Natural Resilience of Families and the Socio-economic Benefits of Informal Care Family carers of people with MND often describe their caring experiences as unrelenting due to the progressive nature of the disease and the hopelessness of recovery. Studies have reported that family carers suffer from anxiety, depression, fatigue, impaired quality of life and reduced social contacts. While the management of physical symptoms in MND is paramount, attending to such family carers’ psychosocial factors is crucial to prevent deterioration in health outcomes. Most individuals with MND live at home, where their psychosocial functioning is intimately connected to the extent and quality of support they receive from family members.

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Notwithstanding the physical, psychological and emotional burden of the disease on family carers, the Deloitte Access Economic Report has quantified the economic disadvantage on families supporting people with MND, who provide an estimate of 7.5 hours of informal care per day. The productivity loss due to such informal care in Australia was estimated to be $68.5 million in 2015, or $32,728 per person, with individuals shouldering most of these costs ($44 million) and government bearing the rest ($24.5 million) (Deloitte Access Economics 2015). Therefore, it is important to design and evaluate effective models of care and find ways to deliver them to families living and caring for someone with MND (Aoun et al. 2017b). Models of care with practical and emotional benefits already provided by MND associations have not been well investigated (Aoun et al. 2018). In order to inform future planning and policies for solutions to the growing demand for family care and the associated challenges encountered by family carers, it is essential to integrate family carers’ needs into service planning. Acknowledgments  We acknowledge the contribution of Ashley Crook to the genetic testing section, and Leanne Jiang for assistance in formatting the references.

References Advance Care Planning Australia (2018). Advance care planning and the law. https://www.advancecareplanning.org.au/for-health-and-care-workers/ legal-requirements Aoun, S.M. (2018). The palliative approach to caring for motor neurone disease: From diagnosis to bereavement. European Journal for Person Centered Healthcare 6 (4): 675–84. Aoun, S.M., L.J. Breen, D. Oliver, R.D. Henderson et al. (2017a). Family carers’ experiences of receiving the news of a diagnosis of Motor Neurone Disease: A national survey. Journal of the Neurological Sciences 372: 144–51. Aoun, S.M., K. Deas, L.J. Kristjanson, and D.W. Kissane (2017b). Identifying and addressing the support needs of family caregivers of people with motor neurone disease using the Carer Support Needs Assessment Tool. Palliative and Supportive Care 15 (1): 32–43. Aoun, S.  M., B.  Rumbold, D.  Howting, A.  Bolleter, and L.J.  Breen (2017c). Bereavement support for family caregivers: The gap between guidelines and practice in palliative care. PLoS One 12 (10): e0184750. Aoun, S.M., A.  Hogden, and L.K.  Kho (2018). “Until there is a cure, there is care”: A person-centered approach to supporting the wellbeing of people with Motor Neurone Disease and their family carers. European Journal for Person Centered Healthcare 6 (2): 320–28.

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Australian Government (2018). National Palliative Care Strategy 2018. https:// www.health.gov.au/internet/main/publishing.nsf/Content/EF57056B DB047E2FCA257BF000206168/$File/12291_PC-Strategy.pdf Australian Human Rights Commission (2015). Face the facts: Cultural diversity. https://www.humanrights.gov.au/our-work/education/face-facts-culturaldiversity Australian Institute of Health and Welfare (2016). Australia’s health 2016. Australia’s health series no. 15. Cat. no. AUS 199. Canberra: AIHW. https:// www.aihw.gov.au/getmedia/f2ae1191-bbf2-47b6-a9d4-1b2ca65553a1/ ah16-2-1-how-does-australias-health-system-work.pdf.aspx Banfield, M., K. Gardner, I. McRae, J. Gillespie et al. (2013). Unlocking information for coordination of care in Australia: A qualitative study of information continuity in four primary health care models. BMC Family Practice 14 (1): 34. Berlowitz, D.J., M.E.  Howard, J.F.  Fiore, S.  Vander Hoorn et  al. (2016). Identifying who will benefit from non-invasive ventilation in amyotrophic lateral sclerosis/motor neurone disease in a clinical cohort. Journal of Neurology, Neurosurgery and Psychiatry 87 (3): 280–86. Carer Gateway (2019). What is respite. https://www.carergateway.gov.au/ respite/what-respite Carer Recognition Act (2010). (Cth) (Austl.). Crook, A., K.  Williams, L.  Adams, I.  Blair, and D.B.  Rowe (2017). Predictive genetic testing for amyotrophic lateral sclerosis and frontotemporal dementia: Genetic counselling considerations. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 18 (7–8): 475–85. Department of Transport (2019). Application for the Taxi Users’ Subsidy Scheme. www.transport.wa.gov.au/mediaFiles/taxis/ODT_F_App_TUSS.pdf Economics, D.A. (2015). Economic analysis of motor neurone disease in Australia Motor Neurone Disease, (November). Fight MND (2019). FightMND. https://fightmnd.org.au/ Goodwin, N., L. Sonola, V. Thiel, and D.L. Kodner (2013). Co-ordinated care for people with complex chronic conditions: Key lessons and markers for success. The King’s Fund UK. ISBN 978-1-909029-19-4. Government, V (2008). Motor neurone disease and palliative care report on the project MND pathway. Health Victoria Government (2019). Voluntary assisted dying. https://www2. health.vic.gov.au/hospitals-and-health-services/patient-care/end-of-lifecare/voluntary-assisted-dying Henderson, R.D., N.  Hutchinson, J.A.  Douglas, and C.  Douglas (2014). Telehealth for motor neurone disease. The Medical Journal of Australia 201 (1): 31. Hogden, A. and A.  Crook (2017). Patient-centered decision making in amyotrophic lateral sclerosis: Where are we? Neurodegenerative Disease Management 7 (6): 377–86.

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Hogden, A., S.M.  Aoun, and P.L.  Silbert (2018). Palliative care in neurology: Integrating a palliative approach to amyotrophic lateral sclerosis care. European Journal of Neurology 6 (1): 68–76. Hogden, A., G.  Foley, R.D.  Henderson, N.  James, and S.M.  Aoun (2017). Amyotrophic lateral sclerosis: Improving care with a multidisciplinary approach. Journal of Multidisciplinary Healthcare 10: 205. James, N., E. Power, A. Hogden, and S. Vucic (2018). Patients’ perspectives of multidisciplinary home-based e-Health service delivery for motor neurone disease. Disability and Rehabilitation Assistive Technology 14 (7): 1–7. MND and Me (2019). MND and me. http://www.mndandme.com.au/ Motor Neurone Disease Australia (2017a). $25 million, 25 milestones: Changing the future of MND. https://www.mndaust.asn.au/Discover-ourresearch/$25-Million,-25-Milestones-Changing-the-future-o.aspx Motor Neurone Disease Australia (2017b). Position statement: Development and approval of drugs to treat motor neurone disease. https://www.mndaust.asn. au/About-us/Policies-and-position-statement/National-policies-andposition-statements/Development-and-approval-of-MND-drugs.aspx Motor Neurone Disease Australia (2018a). MND death statistics. https://www. mndaust.asn.au/Discover-our-research/Latest-research/Statistics.aspx Motor Neurone Disease Australia (2018b). Until there is a cure, there is care. https://www.mndaust.asn.au/News-and-media/State-Association-facts-andfigures.aspx Motor Neurone Disease Australia (2018c). MND support service model. https:// www.mndaust.asn.au/About-us/Policies-and-position-statement/Nationalpolicies-and-position-statements/MND-Support-Service-Model-2018.aspx Motor Neurone Disease Australia (2018d). MND Australia familial MND and genetic testing. http://www.mndaust.asn.au/Documents/Informationresources/MND-Australia-Familial-MND-and-genetic-testing-201.aspx Motor Neurone Disease Australia (2019). Support from state MND associations. https://www.mndaust.asn.au/Find-help/Support-from-state-MNDassociations.aspx Oliver, D.J., G.D. Borasio, A. Caraceni, M. de Visser et al. (2016). A consensus review on the development of palliative care for patients with chronic and progressive neurological disease. European Journal of Neurology 23 (1): 30–38. Productivity Commission (2017). Integrated care, shifting the dial: 5-year productivity review, supporting paper No. 5, Canberra. WA Companion Card (2016). Homepage. http://www.wacompanioncard. org.au/

CHAPTER 3

Public Policy in ALD/MND Care: The Belgian Perspective Evy Reviers, Ludo Vanopdenbosch, Ludo Van Den Bosch, and Philip Van Damme

Abstract  Belgium has a population of 11 million people, which means that there should be 110–220 ALS cases per year and that there are 440 to 880 people living with ALS.  There is no population-based national registry for ALS, but a national database for neuromuscular diseases exists.

Document note organization ALS Liga Belgium is available on www.ALS.be All information on the European Organization for Professionals and Patients with ALS EUpALS is available on www.ALS.eu E. Reviers ALS Liga Belgium, Leuven, Belgium e-mail: [email protected] L. Vanopdenbosch AZ Sint Jan Brugge Oostende, Brugge, Belgium e-mail: [email protected] L. Van Den Bosch • P. Van Damme (*) KU Leuven, Leuven, Belgium e-mail: [email protected]; [email protected] © The Author(s) 2021 R. H. Blank et al. (eds.), Public Policy in ALS/MND Care, https://doi.org/10.1007/978-981-15-5840-5_3

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The multidisciplinary care for patients with ALS and their families is organized in neuromuscular reference centers. Most patients stay at home even in the terminal stages of the disease, thanks to a generous care budget which can be used by patients for home care. Euthanasia is legal in Belgium, and about 25 percent of patients with ALS are thought to plan their end of life this way, mostly at home in a terminal disease stage. ALS Liga Belgium is a very well-organized and active organization, which plays an important role in the care for patients living with ALS, in the public awareness of the disease, in fund raising for research and in defending the rights of ALS patients and their families. Keywords  ALS • Neuromuscular reference center • Care budget • ALS Liga • Euthanasia • Palliative sedation

Incidence, Prevalence and Deaths of ALS/MND in Belgium In Belgium, there is no national registry for ALS/MND.  However, a national database for neuromuscular disorders exists, that is, the Belgian Neuromuscular Disease Registry (BNMDR, https://www.sciensano.be/ en/belgian-neuromuscular-disease-registry-bnmdr) (Roy et  al. 2015). This database is operated by Sciensano, a national institute for science and health, which also is responsible for health and disease monitoring in Belgium. The database was commissioned in 2008 and continues to grow. Data from pediatric and adult patients with neuromuscular conditions followed in one of the seven Neuromuscular Reference Centers in Belgium are collected in this database. The capture of patients continues to grow. According to this database, the prevalence amounts to 8–12/100,000 in the districts with the highest capture rate. The number of new patients is estimated to be around 220 per year, and a similar number of patients die of the disease every year. A recent study reported even slightly higher mortality numbers per year (Maetens et al. 2019). Due to improved multidisciplinary care with nutritional and non-invasive respiratory support, the median survival has increased with a few months over the last decade (Fig. 3.1).

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% Survival

Before 2009 After 2009

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Median survival 33.3 36.8

50

0

0

50

100

150

200

Disease duration (months) Fig. 3.1  Kaplan-Meier curve of patients seen at the University Hospitals Leuven before 2009 (n = 474) and after 2009 (n = 726)

Governmental Agencies Involved in Care There are no governmental committees on ALS/MND in Belgium. Although several benefits for patients with ALS are available, they are not exclusive for ALS patients. Patients living with a rapidly progressive condition can apply for a care budget using a fast-track procedure. Such patients are also supported by assistive goods for mobility and communication by respective agencies of the regions they are living in. The care for patients with neuromuscular disorders, including patients with ALS/MND, is organized through neuromuscular reference centers (NMRCs). There are seven neuromuscular reference centers in Belgium, in Antwerp, Gent/Brugge, Leuven, three in Brussels and one in Liège. The NMRC with the largest cohort of ALS patients is in Leuven (University Hospitals Leuven). It sees about 100 new cases per year, follows about 300 patients and is actively involved in ALS research. NMRCs have multidisciplinary teams typically consisting of administrative workers, specialized nurses, social workers, physiotherapists, occupational therapists, dieticians, speech therapists, psychologists, rehabilitation physicians, pulmonologists and neurologists. The cost of the care is covered by the government. The centers receive a fixed fee per patient, which allows them to organize high-quality care for

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patients and their families. The initiation of non-invasive ventilation is only possible in neuromuscular reference centers. Home care, however, is not supported through this system. Although this network of multidisciplinary reference centers is well-established, probably about one-third of patients stay with their local neurologist and opt not to be offered the possibility of non-invasive ventilation and multidisciplinary care.

Private ALS/MND Organizations and Advocacy Groups ALS Liga Belgium is a non-profit organization founded in 1995, managed by patients and patients’ relatives only. It offers patients with ALS/MND, their families and friends, a diversified service, based upon four pillars: • Stimulating and financing scientific research on ALS. • Informing and providing direct support to patients with ALS/MND and their families. • Defending the rights of patients with ALS/MND at governments and agencies. • Providing free-of-charge high-tech aid goods for mobility and communication. In addition to a national role, the ALS Liga Belgium also plays a prominent role at the international level. It has initiated several international projects, both within and outside Europe, and cooperates actively with the International Alliance of ALS/MND Associations. The ALS Liga Belgium also established EUpALS, the European Organization for Professionals and Patients with ALS. EUpALS takes the interest of European patients with ALS/MND to heart. It creates equal rights for all European ALS/MND patients by providing them better access to research and according information. It especially focuses on harmonizing the European legislation related to research and optimizing the quality of life to the benefit of patients with ALS/MND.

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Policy Associated with ALS/MND Research There is no national funding body specifically devoted to ALS/MND research in Belgium. Research applications can be submitted to general funding agencies such as the Fund for Scientific Research. Typically, such applications will be reviewed by international reviewers, and the final decision will be taken by a panel with expertise in neurological disorders. The amount of public funding for ALS research is therefore not fixed and entirely depends on the quality of the research proposals submitted. The relative contribution from the private sector has increased over the years. Ten years ago it was less than 5 percent of total research budgets, but currently it exceeds 30 percent. The care budget is allocated to neuromuscular reference centers (NMRCs) by the government in the same way as for other patients with neuromuscular conditions. A fixed fee per patient in multidisciplinary follow-­up is provided to the hospital in order to cover the costs of the in-­ hospital care teams. The care at home is not covered through this system, but through direct financial support to patients with high care needs. Since 2014, the Belgian government also has funded ALS/MND care by providing a fixed yearly budget of 120,000 euros (US$133,000) for two full time equivalent liaison workers. They support patients with ALS/ MND in their homes. In particular, the liaison workers coordinate home care by interacting with all stakeholders especially in acute situations. This service is free of charge for the patients. Fundraising from the general public at the national level is done by ALS Liga Belgium, with multiple fundraising campaigns and initiatives, often local initiatives, but sometimes also in collaboration with other European countries in international events. At the local level at the University of Leuven, there are three ALS funds that raise money locally for research purposes.

Public and Media Perceptions of ALS/MND The knowledge of the general public about ALS/MND has increased over the last years. The Ice Bucket Challenge contributed to this awareness as well as the continuous efforts of ALS Liga Belgium. For instance, close collaboration of ALS Liga Belgium with the production team of the soap series THUIS recently resulted in a character that was suffering from

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ALS/MND. In this way, the general public became aware of ALS/MND in the TV season in 2018–19.

Care of ALS/MND Patients in Belgium The default pathway for the organization of care for patients with ALS is home care, organized by the patients and their families. The multidisciplinary teams have an advisory role and help with the organization of the care. Most patients stay at home throughout their disease trajectory. By using a home care budget (see later in the chapter), many patients can organize their care at home even in the later stages of the disease when they are completely dependent on the help of others. Less than 10 percent of patients are cared for in hospices, usually as care needs have become too high at home. Patients without family, or patients with care demands that exceed the capacity of the local caregivers, can be admitted to institutional care. However, most hospices are not equipped to handle patients on non-­ invasive or invasive ventilation and typically have a population of elderly people. The use of non-invasive ventilation is usually not hampered by a lack of care at home. So long as patients have supervision 24 hours a day from caregivers that have had training on the use of non-invasive ventilation, the option to start non-invasive ventilation is available. Invasive ventilation is rarely initiated for several reasons, such as personal preferences and cultural reasons, but also because of the burden of the home care. The patient is responsible to organize the home care for invasive ventilation, and this requires medically trained caregivers 24 hours per day. As this is not reimbursed in Belgium, many patients do not undergo tracheostomy, and probably less than 1 percent of patients eventually become invasively ventilated. There are no dedicated homes for people living with ALS. In the framework of a National Convention, however, some hospices have dedicated beds for patients that have high care needs, for example, those that require ventilation when home care is no longer possible. In the final stage of the disease, the role of the general practitioner becomes very important because patients often are no longer able to travel to the multidisciplinary clinics. Palliative care, palliative sedation and euthanasia are possible at home under the supervision of the general practitioner. As a result, few patients die in hospitals in neurology wards or in palliative care units.

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Composition of Caregivers: Informal, Formal (Paid) The team of caregivers can be composed of informal and formal members. In many cases, close relatives take part in the care of the patients. There are legal systems that allow working part-time to care for a close family member. Patients can also rely on formal home nurses for help with washing, clothing, wound-care, tube feeding and so forth. Such home nurses can come for brief visits one to three times per day, but there are challenges to have the visits organized at fixed time points. These formal caregivers can be hired through the home care budget (see later). Apart from these systems, there are local initiatives to support ill people at home. Despite the different care options, the organization of care can be quite challenging for patients in later stages of the disease when they need a permanent caregiver. Once the patient depends on a caregiver at night, such as for pressure area care or to cope with aspiration or the relief of cramps, the burden increases. In practice, the search for informal or formal caregivers working at night is difficult. Governmental Aid for Family Caregivers In Belgium, governmental aid for family caregivers is provided by respective agencies from the region in which they live, each with distinct regulations. In Flanders, the Flemish Agency for Persons with a Disability (VAPH) introduced a personal budget (PVB) that amounts to 60,778 € (US$75,400) per year for persons with a progressive degenerative disorder. Patients with ALS/MND can apply via a fast-track procedure. The personal budget can be used to organize the needed care and support by, amongst others, the family caregivers. Inhabitants of Flanders who are not eligible to receive this personal budget can apply at their health insurance fund for a premium for family care of 130 € (US$145) per month. In Wallonia, the Walloon Agency for Persons with a Disability (AVIQ) also provides personal budgets (BAP) to persons with a disability, which is set between 1000 € (US$1100) and 35,000 € (US$ 39,000) per year. In the German community, the agency Dienststelle für Selbestimmtes Leben informs patients with ALS/MND about the financial aid and respite care that is available to their citizens.

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Access to Assistive Technologies Patients with ALS/MND in Belgium have access to assistive technologies through specific procedures and conditions depending on the region in which they live. In Flanders, from January 2019 a new leasing system is in place via the Vlaamse Sociale Bescherming (VSB; Flemish Social Protection) for mobility aids such as walkers, manual or power wheelchairs and scooters. Persons with a progressive degenerative disease, including ALS/MND, can apply by a fast-track procedure. For a (partial) refund of purchases of other aid goods (transportation tools, electric beds, communication devices) as well as adaptations of their home, persons living in the Flemish Region can under certain conditions apply at the agency VAPH. In Wallonia and the capital city Brussels, the respective agencies AVIQ and PHARE provide a system of reimbursements of purchases of assistive technologies. However, no fast-track procedures are available for people with ALS/MND. Finally, ALS Liga Belgium has the specific service ALS Mobility & Digitalk (ALS M&D) dedicated to rent assistive technologies for mobility and communication to patients with ALS/MND. This lending service is free of charge and open to those patients who do not qualify to obtain the assistive goods via the systems set up by the respective regional agencies.

Status of Multidisciplinary Team Care and Clinics The multidisciplinary teams (neuromuscular reference centers) are funded by the state. The teams will receive a fixed sum per annum to organize the care for the patients in an ambulant setting. Home visits are possible, especially by occupational therapists, to advise on the use of aids and to advise on refurbishments to the home needed to make the care at home feasible. Home visits on a regular basis, by a specialized nurse, unfortunately are not covered through the system of neuromuscular reference centers. The multidisciplinary teams are in close contact with the general practitioner and help to get the care at home organized. At the same time, they monitor nutritional and respiratory status and advise on the use of tube feeding, noninvasive ventilation and so forth. Typically, patients with ALS are seen every two to six months, depending on the rate of disease progression. Between visits, they are in regular contact with a specialized nurse for further questions. For non-medical support, patients can contact patient organization ALS Liga Belgium. A liaison person of ALS Liga Belgium supports patients with ALS/MND in their home situation in acute situations.

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Right to Try Unapproved Drugs for ALS/ MND Patients There is no national legislation that supports the right to try in Belgium. However, in Belgium (as in the rest of the European Union), laws supporting the use of experimental drugs in a compassionate use or named patient format prior to registration exist. For less expensive experimental drugs, any physician can prescribe drugs that are not as yet approved by EMA and that are not on the market in Belgium. However, experimental drugs with a high price are problematic unless the company is willing to provide the drug for free in an early access program. If this is not the case, it is deemed unethical by most physicians and ethics committees to let the patient cover the cost of the treatment. There is no legal obligation for physicians to prescribe experimental drugs, and most patients understand that the use of experimental drugs outside the context of a clinical trial can be harmful. ALS centers and the ALS Liga Belgium attempt to communicate in a uniform manner about experimental therapies to avoid misunderstanding by patients and their caregivers. Participation in clinical trials is the preferred option to offer selected patients access to non-approved treatment in a safe manner. Off-­ label symptomatic medication is prescribed for some indications such as drooling.

Genetic Testing for ALS/MND Many patients in Belgium are interested to know if they carry pathogenic mutations in known ALS genes. Also, in patients without a positive family history, gene testing is frequently offered. The genetic testing in Belgium is almost completely covered by the health care system. There are fixed tariffs for gene tests, and the proportion of the bill that is charged to the patient is small. For example, to get a diagnostic gene test for ALS, which currently includes testing for C9orf72, SOD1, TARDBP and FUS, the total cost is 570 € (US$ 630), but only 8.65 € (US$ 9.50) is charged to the patient. In familial cases, 55 percent have a C9orf72 expansion, 20 percent a SOD1 mutation and less than 5 percent a TARDBP or FUS mutations. In about 7 percent of sporadic patients, a C9orf72 repeat expansion is found (Debray et al. 2013).

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Whenever pathogenic mutations are found, family members of ALS patients are offered genetic counseling. Individuals over 18 years old can undergo a predictive gene test after genetic counseling, which is routinely provided. This is mostly carried out in people who are planning to have children. This gene test is performed in duplicate on two independent blood samples and costs 2 × 158.52 € (US$ 175), of which 2 × 8.65 € (US$ 19) is charged to the person that requests the test. Mutation carriers can opt to prevent transmission of disease-causing mutations by in vitro fertilization and pre-implantation genetic diagnostics. Up to six attempts are reimbursed by the health care system.

Access to Palliative and Hospice Care Belgium has a variety of structures and services for palliative care that can be provided at home, in day centers and in palliative care units in hospitals and nursing homes. Although there is sufficient access to palliative care units and hospices, this option is not widely used in Belgium. As pointed out earlier, most patients receive palliative care at home and prefer to stay at home until the very end. If the care burden exceeds the capacity of the caregivers, a difficult decision to transfer the patient must be taken. Patients with ALS all have access to the palliative status, which gives them additional rights for support. In Belgium, the palliative status is not only for the terminal disease stage. The term supportive care is preferred over palliative care as it enables support throughout all stages of the disease from diagnosis onwards. The percentage of patients enrolled in palliative care is influenced by the euthanasia law. Although there are no reliable numbers on the actual percentage of patients who die at home in Belgium, it has been assumed to be high. A recent study, however, suggests that it is only around 40 percent (Maetens et al. 2019). Some patients are admitted to the hospital in the terminal disease stage with respiratory infections, respiratory failure or because the situation at home becomes too strenuous. Of those, estimated to be less than 15 percent, most will die in the neurology ward and a small proportion will be admitted to a palliative care unit.

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Advance Directives and Withholding or Withdrawing Life-Extending Interventions Advance directives (ADs) are an important part of the management of patients living with ALS. There is a legally binding possibility for patients to register the treatments they no longer want to receive and to describe their wishes in case of a sudden cardiac arrest, admission on intensive care, coma and so forth. The patient’s ADs can be registered on a plastic card that is stored in their wallet. In addition, most hospitals have internal procedures for registering the ADs of patients. It is observed in Belgium that most patients in the later stages of the disease opt not to be resuscitated in case of an emergency, not to be intubated in case of respiratory failure and not to be transferred to an intensive care unit. Probably less than 2 percent of patients opt for invasive ventilation. Withdrawing unwanted life-­ extending interventions, including mechanical ventilation, is possible. Even when patients never indicated their wishes about invasive ventilation, it is possible to stop mechanical support after discussing this with the patient, or if this is no longer possible, with the close relatives.

Palliative Sedation and Euthanasia In Belgium, palliative sedation and euthanasia are legal. In 2002, the euthanasia law was passed. Prior to passing the law by the federal parliament, the ALS Liga Belgium provided substantial input to the policy-­ makers and made adaptations to the draft text. It states that under certain circumstances, physicians who carry out euthanasia will not be prosecuted. Legally, euthanasia is defined as the medical act to intentionally end the life of a patient at his or her request. Patients can only submit a written request for euthanasia if they are conscious and mentally competent, if they have a medical condition that cannot be cured and if they have persistent unsupportable, untreatable physical or psychological suffering. The patient’s decision should be taken freely, without pressure from their surroundings and after careful consideration. The physician should discuss other options, such as palliative care, and make sure that all conditions are fulfilled. If the patient is expected to die within a reasonable time, only one additional independent physician’s advice is sought. If this is not the case, there should be a waiting period of at least one month between the request and the act of euthanasia, and the advice of a third independent physician is mandatory. The physician who

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carries out the euthanasia is obliged to report to a federal committee which checks if all requirements were fulfilled. Every two years, a report on the use of euthanasia is made available publicly. Between 2014 and 2017, on average 52 ALS patients per year died per year after euthanasia. This corresponds roughly to about 25 percent of the ALS deaths each year. Because there is no obligation to report on the use of palliative care and palliative sedation, it is not clear what proportion of patients makes use of these possibilities. Organ donation following euthanasia is possible, but only at the explicit request of the ALS patient. The euthanasia is then performed in hospital, followed by a time-out hands-off waiting time of five minutes after the cessation of heart beating, after which organs can be procured according to a non–heart-beating donor procedure. The ethical and practical difficulties are significant, and independence between the euthanasia team and the organ transplantation team is essential (Bollen et al. 2016).

Factors Unique to Belgium In comparison with other European countries, the following trends are observed in Belgium: (1) many patients want gene testing to make sure that their children can make informed decisions about family planning, (2) many patients want to stay at home as long as possible, (3) very few opt for mechanical ventilation and (4) euthanasia is legal, and a considerable proportion of patients makes use of this possibility. Factors that contribute to this unique situation are heterogeneous and cultural, social and economic in nature. The contribution of religious factors has decreased over the last decades. Patient autonomy, living with family and quality of life are typically highly valued. Most patients actively plan the end-of-life management themselves. Economic factors, such as reimbursement for genetic testing and personal care budgets, facilitate the use of gene testing (also in sporadic patients) and reduce the number of patients who are admitted in hospices for care. The Belgian regions (Flanders, Wallonia, Brussels, the German community) differ somewhat in terms of culture, social cohesion, religion and economy. Therefore, national decision-making is often a compromise made among the regions, or made solely on a regional level. As a result, decision-making on the national level mostly takes more time than at the regional level.

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Conclusions: ALS/MND Policy in Belgium In Belgium, there are many options for the care of ALS/MND patients and support for their families. Some regulations are unique and therefore well appreciated, like fast-track application procedures. However, the Belgian landscape of the organization of care is highly scattered over different agencies and institutions and is differently organized in the various regions of the country, and this makes it hard for patients to find their way. For many of the applications there is a huge administrative burden, sometimes long waiting lists and sometimes patients are not eligible due to age restrictions. The organization of care would benefit from a more harmonized system in which patients can address their questions and apply for support to a single agency or institute. At the level of research, the situation in Belgium could improve if dedicated funding schemes for ALS research, including clinical research, would exist. Furthermore, the research foundation is geared toward more fundamental research, and it is difficult to receive a grant for more clinically oriented studies.

References Bollen, J., R. Ten Hoopen, D. Ysebaert, W. van Mook, and E. van Heurn (2016). Legal and ethical aspects of organ donation after euthanasia in Belgium and the Netherlands. Journal of Medical Ethics 42: 486–89. Debray, S., V. Race, V. Crabbe, S. Herdewyn, G. Matthijs, A. Goris, B. Dubois, V. Thijs, W. Robberecht, and P. Van Damme (2013). Frequency of C9orf72 repeat expansions in amyotrophic lateral sclerosis: A Belgian cohort study. Neurobiol Aging 34: 2890, e2897–2890, e2812. Maetens, A., L. Deliens, J. De Bleecker, A. Caraceni, M. De Ridder, K. Beernaert, and J. Cohen (2019). Healthcare utilization at the end of life in people dying from amyotrophic lateral sclerosis: A retrospective cohort study using linked administrative data. Journal of the Neurological Sciences 406: 116444. Roy, A.J., P. Van den Bergh, P. Van Damme, K. Doggen, V. Van Casteren, and B.S. Committee (2015). Early stages of building a rare disease registry, methods and 2010 data from the Belgian Neuromuscular Disease Registry (BNMDR). Acta Neurologica Belgica 115: 97–104.

CHAPTER 4

Amyotrophic Lateral Sclerosis in Brazil Tauana Bernardes Leoni and Marcondes C. França Jr.

Abstract  Brazil is a country of continental dimensions, with remarkable regional heterogeneity which greatly influences the distribution of ALS as well as the standards of care across the nation. The overall prevalence and phenotypic presentation of ALS in Brazil is like that of Europe and North America. However, the genetic basis of the illness seems to be different; mutations in VAPB indeed account for a high proportion of familial ALS in Brazil. The Brazilian public healthcare system has various policies for people with ALS that include dispensing riluzole, providing non-invasive ventilatory support and wheelchairs and enabling rehabilitation. Unfortunately, these are often not implemented in many regions of the country. Much work still needs to be done to improve the general care of patients with ALS across Brazil. Keywords  Amyotrophic lateral sclerosis • Brazil • Public healthcare • Epidemiology of ALS

T. B. Leoni • M. C. França Jr. (*) University of Campinas, Campinas, Brazil e-mail: [email protected]; [email protected] © The Author(s) 2021 R. H. Blank et al. (eds.), Public Policy in ALS/MND Care, https://doi.org/10.1007/978-981-15-5840-5_4

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Introduction Brazil is a country of continental dimensions, with remarkable heterogeneity among regions, particularly in terms of socio-economic development and ethnic background. In general, southern Brazil has better social indicators, whereas the scenario in the northern and north-eastern parts of the country is worse. The Brazilian population results from a mixture of Caucasian, African, Japanese and Amerindian descendants. However, the relative proportions of each race are not the same in the different regions of the country. In the south, there was relatively recent immigration flux from Europe, mostly Italian and German, and in this region, there is a relatively higher contribution of people from Caucasian descent. In contrast, the influence of Africans and Amerindians is much higher in the north and north-eastern regions (Pena et al. 2009). We believe that readers must be familiar with these introductory concepts about Brazil in order to understand the epidemiology and the current standards of care of ALS across the country.

ALS in Brazil: Overview The general profile of Brazilian patients suffering from ALS is in many ways like that reported in European and North American series. However, recent publications have also highlighted some local specificities of the disease, particularly related to the genetic epidemiology (Chadi et al. 2017). There are few published surveys devoted to the epidemiology of ALS in Brazil. Perhaps, the most comprehensive study was published by Moura et al. (2016). These authors looked at death certificates across the country to uncover ALS-related burden in the period between January 2004 and December 2013. They found that the ALS-related death rate in Brazil ranged from 0.36/100,000  in 2004 to 0.58/100,000  in 2013. Considering adjusted mortality rates, they were able to estimate the incidence of ALS in persons over 20 years of age to be 0.61 to 0.89/100,000 and that in persons above 45 years of age 1.77 to 2.3/100,000, with clear predominance in Caucasians. In this scenario, the odds ratio of dying due to ALS was almost three times higher in Caucasians than in all other races. This seemingly Caucasian predominance is also reflected by the geographical distribution of ALS-related deaths, which is higher in the southeast and southern regions, with more than half of all ALS-related deaths occurring in these regions. Matos et  al. used a similar approach—using

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death certificate data—to estimate ALS-related death rates in the largest city of Brazil (São Paulo). The estimates were like those previously found, ranging from 0.44 cases per 100,000  in 2002 to 0.76 per 100,000  in 2006 (Matos et al. 2011). Another epidemiological study was performed by Linden-Junior et al. (2013) in the city of Porto Alegre, the capital of the southernmost state of Brazil. These authors contacted all active neurologists and neurosurgeons in the city to gather data about the ALS patients followed by each of them. Using this approach, they reached a prevalence of five cases per 100,000 residents in Porto Alegre, with similar distribution between men and women. In addition, prevalence was found to increase with age, reaching the peak values between 70 and 79 years (30.5/100,000). Following a different approach, a group at the University of Campinas (UNICAMP) also obtained prevalence and incidence estimates regarding ALS. We analyzed riluzole dispensing data, which in Brazil is only approved to treat ALS and is only given by the public health system. We estimated in the city of Campinas an incidence of 1.49/100,000/year and a prevalence of 3.92/100,000 (Vicente dos Anjos and França Jr 2013). Detailed phenotypic characterization of the published Brazilian cohorts is shown in Table 4.1. Overall, the clinical presentation of Brazilian patients with ALS is similar to that found in European/North American individuals (Loureiro et  al. 2012). The only remarkable difference is the age at onset, which seems to be younger in Brazil. Cognitive and behavioral impairment have been recognized only recently in Brazil. Branco et  al. found that only 5 percent of all patients met the criteria for Table 4.1  Phenotypic characterization of Brazilian patients with ALS Authors (year) Number of subjects Mean age at onset (years) Men (%) Spinal (classical) Bulbar Diplegic Hemiplegic Progressive lateral sclerosis Pseudopolyneuritic Progressive muscular atrophy

de Castro-Costa et al. (1999) Loureiro et al. (2012) Fortaleza (Northeastern) Rio de Janeiro (Southeastern) 78 42.0 51 (65.4%) 93% 2.2% – – – – 2.2%

227 53.6 84 (37%) 64.8% 30.4% 1.3% 0.4% – 2.2% 2.2%

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frontotemporal dementia (FTD), but 20 percent had definite evidence of cognitive impairment (Branco et al. 2017). Genetic aspects of ALS have gained much attention recently. Overall, 10 percent of all patients have familial ALS (fALS), which (often) segregates an autosomal dominant trait and is caused by pathogenic variants in approximately 20 genes (Renton et al. 2014). In European cohorts, mutations in C9orf72 and SOD1 account for the majority of fALS cases (Zou et al. 2017). The genetic epidemiology of fALS appears to be slightly different in Brazil. Chadi et  al. evaluated 31 unrelated families from São Paulo and found that these two genes explained approximately 20 percent of them (Chadi et al. 2017). Interestingly, the p.Pro56Ser variant at VAPB was by far the most frequent genetic cause of ALS in this tertiary hospital-­ based sample from southeastern Brazil (46.3% of all cases). This specific subtype of the disease is named familial ALS type 8 and was first described in Brazilian families (Nishimura et  al. 2004). Up until now, very few patients outside Brazil have been reported. It is characterized by predominant lower motor neuron involvement and relatively slow progression compared to other forms of fALS. Tremor and autonomic dysfunction are other conspicuous and distinctive manifestations associated to VAPB-­ related ALS (Marques et al. 2006). Recently, in a large multicentric study devoted to investigating the frequency of C9orf72 mutations in Brazilian patients with either ALS or FTD, Cintra et al. (2018) found that the highest frequency of C9orf72 mutations occurred in the group that presented both FTD and ALS (50% of familial and 17.6% of sporadic cases). For patients with pure ALS, the frequency was 11.8 percent for familial and 3.6 percent of sporadic cases. These numbers are much smaller than those from northern Europe, and again indicate that the genetic underpinnings of ALS have geographical/ ethnical differences.

Organization of the Healthcare System in Brazil The healthcare system in Brazil includes both governmental and private institutions. The public healthcare system is known as Unified Health System (SUS, acronym in Portuguese). Prior to reforms accomplished in 1988, only citizens who contributed to the social security system were able to receive public healthcare services. Today, every Brazilian citizen has access to healthcare, which is considered a constitutional right. This is clearly expressed in the Federal Constitution of 1988, Article 196, which

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states that health is a “right of all” and a “duty of the State”. This directive is regulated by Law 8.080/1990, which operationalizes public healthcare. Public healthcare is based on three basic principles: universal access, equity and integrated care. This means that the system is designed to assist everyone, to provide the amount/type of care tailored for each individual need and to offer all types of medical care, such as mental care, rehabilitation, preventive services and complex surgeries. By June of 2019, there were 47,125,850 individuals with private healthcare insurance across the country, corresponding to 35.2 percent of the total population. The remaining 64.8 percent rely on the public system. There are variations within the country, but as a rule, private care is better than public care. The relative proportions are rather heterogeneous, and some states have a higher percentage of private insurance coverage than others. Notably, the poorer states from the north have less private coverage and depend largely on SUS (Agência Nacional de Saúde Suplementar 2019a, b; Instituto Brasileiro de Geografia e Estatística (IBGE) 2014, 2019).

Public Policies for ALS Patients in Brazil The vast majority of the population depends entirely on public healthcare. The Ministry of Health has issued a document to guide diagnostic and therapeutic measures for ALS patients (the last updated version is from 2015), with riluzole, non-invasive ventilatory assistance and some homecare services available within the public system. Currently, there are three FDA-approved drugs for ALS, two of them for disease-modifying treatment (riluzole and edaravone) and one for symptomatic treatment (Nuedexta for pseudobulbar affect). In Brazil, only riluzole is approved by the local regulatory agency ANVISA.  This greatly limits access of the other two drugs for Brazilian patients in general. Rare patients are on edaravone by means of compassionate use; the high purchase and import costs, however, are major concerns. SUS provides riluzole free of charge to all patients that meet the criteria for definite or probable ALS (El Escorial). The only required documents are a medical prescription and the results of the medical tests that confirm the diagnosis of ALS—nerve conduction studies +EMG (Federal Act 1151, 11 November 2015). There is no clear definition about when and for which patients to stop the medication. Several medicines for symptomatic relief (e.g., cramps, pain, sleep disorders) are available in the public system and easily accessible for patients once they have a medical prescription. As of 2008, the public healthcare

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system provides non-invasive ventilatory assistance in accordance to Federal Act 1370 of 3 July 2008 that established the Non-Invasive Ventilatory Assistance Program for Carriers of Neuromuscular Diseases. For ALS patients, the inclusion criteria for providing supportive ventilatory devices are the presence of clinical or laboratorial (PaCO2 >45 mmHg and/or persistent SpO2